Original source

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

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

Chromosome 4:1002087 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM960875

Most severe consequence
Clinical significance

Synonyms

LSDB 6457

This variation has 6 HGVS names - click the plus to show

4:g.1002087G>A
ENST00000514224.1:c.502G>A
ENSP00000425081.1:p.Ala168Thr
ENST00000514698.2:n.898G>A
ENST00000247933.5:c.898G>A
ENSP00000247933.4:p.Ala300Thr

Variation displays