Original source

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

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

Chromosome 8:31090843 (forward strand) | View in location tab

Most severe consequence
Clinical significance

Synonyms

LSDB 12757

This variation has 7 HGVS names - click the plus to show

8:g.31090843A>T
ENST00000521620.2:n.363A>T
ENST00000298139.5:c.1730A>T
ENSP00000298139.5:p.Lys577Met
LRG_524:g.62582A>T
LRG_524t1.1:c.1730A>T
LRG_524p1.1:p.Lys577Met

Variation displays