Canonical Allele Identifier: CA425627759
Gene: SRD5A2 HGNC NCBI

Linked Data

gnomAD v4: 2-31580982-C-A
MyVariant Identifiers: chr2:g.31806051C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31580982C>A , CM000664.2:g.31580982C>A GRCh38
NC_000002.11:g.31806051C>A , CM000664.1:g.31806051C>A GRCh37
NC_000002.10:g.31659555C>A NCBI36
NG_008365.1:g.4990G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.1:c.-82G>T ENSP00000477587.1:n.-82G>T
XM_011533068.1:c.-82G>T XP_011531370.1:n.-82G>T
XM_011533070.1:c.27-47216G>T XP_011531372.1:n.27-47216G>T
XM_011533071.1:c.27-47216G>T XP_011531373.1:n.27-47216G>T
XM_011533072.1:c.27-47216G>T XP_011531374.1:n.27-47216G>T
XM_011533072.2:c.27-47216G>T XP_011531374.1:n.27-47216G>T