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 1:173914582 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM970122

Most severe consequence
Clinical significance

Synonyms

LSDB 380

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

1:g.173914582A>G
ENST00000494024.1:n.605T>C
ENST00000367698.3:c.379T>C
ENSP00000356671.3:p.Cys127Arg
ENST00000487183.1:n.84T>C
ENST00000617423.2:c.379T>C
ENSP00000478688.1:p.Cys127Arg

Variation displays