Canonical Allele Identifier: CA1242197452
Gene: SRD5A2 HGNC NCBI

Linked Data

dbSNP Id: rs1572629262

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31529491C>T , CM000664.2:g.31529491C>T GRCh38
NC_000002.11:g.31754561C>T , CM000664.1:g.31754561C>T GRCh37
NC_000002.10:g.31608065C>T NCBI36
NG_008365.1:g.56481G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.548-34G>A MANE Select ENSP00000477587.1:n.548-34G>A
ENST00000622030.1:c.548-34G>A ENSP00000477587.1:n.548-34G>A
NM_000348.3:c.548-34G>A NP_000339.2:n.548-34G>A
XM_011533069.1:c.326-34G>A XP_011531371.1:n.326-34G>A
XM_011533070.1:c.293-34G>A XP_011531372.1:n.293-34G>A
XM_011533071.1:c.293-34G>A XP_011531373.1:n.293-34G>A
XM_011533072.1:c.293-34G>A XP_011531374.1:n.293-34G>A
XM_011533069.2:c.326-34G>A XP_011531371.1:n.326-34G>A
XM_011533072.2:c.293-34G>A XP_011531374.1:n.293-34G>A
NM_000348.4:c.548-34G>A MANE Select NP_000339.2:n.548-34G>A