Canonical Allele Identifier: CA425627708

Gene: SRD5A2

Linked Data

• dbSNP Id: rs1214587384
• gnomAD v2: 2-31806041-G-A
• gnomAD v3: 2-31580972-G-A
• gnomAD v4: 2-31580972-G-A
• MyVariant Identifiers: chr2:g.31806041G>A (hg19) ; chr2:g.31580972G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31580972G>A , CM000664.2:g.31580972G>A	GRCh38
NC_000002.11:g.31806041G>A , CM000664.1:g.31806041G>A	GRCh37
NC_000002.10:g.31659545G>A	NCBI36
NG_008365.1:g.5000C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000622030.1:c.-72C>T	ENSP00000477587.1:n.-72C>T
XM_011533068.1:c.-72C>T	XP_011531370.1:n.-72C>T
XM_011533070.1:c.27-47206C>T	XP_011531372.1:n.27-47206C>T
XM_011533071.1:c.27-47206C>T	XP_011531373.1:n.27-47206C>T
XM_011533072.1:c.27-47206C>T	XP_011531374.1:n.27-47206C>T
XM_011533072.2:c.27-47206C>T	XP_011531374.1:n.27-47206C>T