Canonical Allele Identifier: CA346598157
Gene: SRD5A2 HGNC NCBI

Linked Data

gnomAD v4: 2-31531371-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31531371C>A , CM000664.2:g.31531371C>A GRCh38
NC_000002.11:g.31756441C>A , CM000664.1:g.31756441C>A GRCh37
NC_000002.10:g.31609945C>A NCBI36
NG_008365.1:g.54601G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.547G>T MANE Select ENSP00000477587.1:p.Gly183Cys
ENST00000622030.1:c.547G>T ENSP00000477587.1:p.Gly183Cys
NM_000348.3:c.547G>T NP_000339.2:p.Gly183Cys
XM_011533069.1:c.325G>T XP_011531371.1:p.Gly109Cys
XM_011533070.1:c.292G>T XP_011531372.1:p.Gly98Cys
XM_011533071.1:c.292G>T XP_011531373.1:p.Gly98Cys
XM_011533072.1:c.292G>T XP_011531374.1:p.Gly98Cys
XM_011533069.2:c.325G>T XP_011531371.1:p.Gly109Cys
XM_011533072.2:c.292G>T XP_011531374.1:p.Gly98Cys
NM_000348.4:c.547G>T MANE Select NP_000339.2:p.Gly183Cys