Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
A/G | Ancestral: A | Ambiguity code: R
Location

Chromosome 19:35908227 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM025344

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 12428, 2010_April_001_118_TYROBP_604142_0003

This variation has 19 HGVS names - click the plus to show

19:g.35908227A>G
ENST00000544690.3:c.2T>C
ENSP00000445332.1:p.Met1?
ENST00000587837.2:c.2T>C
ENSP00000465081.1:p.Met1?
ENST00000586946.1:c.2T>C
ENSP00000465656.1:p.Met1?
ENST00000424586.4:c.2T>C
ENSP00000402371.3:p.Met1?
ENST00000589517.1:c.2T>C
ENSP00000468447.1:p.Met1?
ENST00000262629.5:c.2T>C
ENSP00000262629.3:p.Met1?
ENST00000585626.1:n.69T>C
ENST00000585901.3:c.2T>C
ENSP00000468608.1:p.Met1?
LRG_607:g.5058T>C
LRG_607t1.1:c.2T>C
LRG_607p1.1:p.Met1?

Variation displays