Canonical Allele Identifier: CA346597984
Gene: SRD5A2 HGNC NCBI

Linked Data

gnomAD v4: 2-31529378-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31529378C>T , CM000664.2:g.31529378C>T GRCh38
NC_000002.11:g.31754448C>T , CM000664.1:g.31754448C>T GRCh37
NC_000002.10:g.31607952C>T NCBI36
NG_008365.1:g.56594G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000622030.2:c.627G>A MANE Select ENSP00000477587.1:p.Trp209Ter
ENST00000622030.1:c.627G>A ENSP00000477587.1:p.Trp209Ter
NM_000348.3:c.627G>A NP_000339.2:p.Trp209Ter
XM_011533069.1:c.405G>A XP_011531371.1:p.Trp135Ter
XM_011533070.1:c.372G>A XP_011531372.1:p.Trp124Ter
XM_011533071.1:c.372G>A XP_011531373.1:p.Trp124Ter
XM_011533072.1:c.372G>A XP_011531374.1:p.Trp124Ter
XM_011533069.2:c.405G>A XP_011531371.1:p.Trp135Ter
XM_011533072.2:c.372G>A XP_011531374.1:p.Trp124Ter
NM_000348.4:c.627G>A MANE Select NP_000339.2:p.Trp209Ter