Canonical Allele Identifier: CA346598192
Gene: SRD5A2 HGNC NCBI

Linked Data

gnomAD v4: 2-31531387-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31531387G>T , CM000664.2:g.31531387G>T GRCh38
NC_000002.11:g.31756457G>T , CM000664.1:g.31756457G>T GRCh37
NC_000002.10:g.31609961G>T NCBI36
NG_008365.1:g.54585C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000622030.2:c.531C>A MANE Select ENSP00000477587.1:p.Ser177Arg
ENST00000622030.1:c.531C>A ENSP00000477587.1:p.Ser177Arg
NM_000348.3:c.531C>A NP_000339.2:p.Ser177Arg
XM_011533069.1:c.309C>A XP_011531371.1:p.Ser103Arg
XM_011533070.1:c.276C>A XP_011531372.1:p.Ser92Arg
XM_011533071.1:c.276C>A XP_011531373.1:p.Ser92Arg
XM_011533072.1:c.276C>A XP_011531374.1:p.Ser92Arg
XM_011533069.2:c.309C>A XP_011531371.1:p.Ser103Arg
XM_011533072.2:c.276C>A XP_011531374.1:p.Ser92Arg
NM_000348.4:c.531C>A MANE Select NP_000339.2:p.Ser177Arg