Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W
Location

Chromosome 15:38299471 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM093928

Most severe consequence
Clinical significance

Synonyms

LSDB 16212

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

15:g.38299471T>A
ENST00000561317.1:c.68T>A
ENSP00000453680.1:p.Val23Asp
ENST00000561205.1:n.469T>A
ENST00000299084.5:c.131T>A
ENSP00000299084.4:p.Val44Asp

Variation displays