Canonical Allele Identifier: CA767792687
Gene: SRD5A2 HGNC NCBI

Linked Data

dbSNP Id: rs1189978032
gnomAD v3: 2-31586738-C-A
gnomAD v4: 2-31586738-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31586738C>A , CM000664.2:g.31586738C>A GRCh38
NC_000002.11:g.31811807C>A , CM000664.1:g.31811807C>A GRCh37
NC_000002.10:g.31665311C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011533070.1:c.27-52972G>T XP_011531372.1:n.27-52972G>T
XM_011533071.1:c.27-52972G>T XP_011531373.1:n.27-52972G>T
XM_011533072.1:c.27-52972G>T XP_011531374.1:n.27-52972G>T
XM_011533072.2:c.27-52972G>T XP_011531374.1:n.27-52972G>T