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 11:118344424 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM920137 ; PhenCode CD3Gbase_HSTCR3G1:g.1380A>G (A/G)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 5527, 2010_April_001_026_CD3G_186740_0001

This variation has 14 HGVS names - click the plus to show

11:g.118344424A>G
ENST00000392883.3:c.-180A>G
ENST00000292144.5:c.1A>G
ENSP00000292144.4:p.Met1?
ENST00000527777.2:n.81A>G
ENST00000528540.2:n.39A>G
ENST00000532917.1:c.1A>G
ENSP00000431445.1:p.Met1?
ENST00000532903.1:n.18A>G
ENST00000533462.2:n.81A>G
LRG_37:g.3321T>C
LRG_39:g.5081A>G
LRG_39t1.1:c.1A>G
LRG_39p1.1:p.Met1?

Variation displays