Canonical Allele Identifier: CA45136012

Gene: SRD5A2

Linked Data

• dbSNP Id: rs1030279201
• gnomAD v3: 2-31526558-A-C
• gnomAD v4: 2-31526558-A-C
• MyVariant Identifiers: chr2:g.31751628A>C (hg19) ; chr2:g.31526558A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31526558A>C , CM000664.2:g.31526558A>C	GRCh38
NC_000002.11:g.31751628A>C , CM000664.1:g.31751628A>C	GRCh37
NC_000002.10:g.31605132A>C	NCBI36
NG_008365.1:g.59414T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.699-296T>G MANE Select	ENSP00000477587.1:n.699-296T>G
ENST00000622030.1:c.699-296T>G	ENSP00000477587.1:n.699-296T>G
NM_000348.3:c.699-296T>G	NP_000339.2:n.699-296T>G
XM_011533069.1:c.477-296T>G	XP_011531371.1:n.477-296T>G
XM_011533070.1:c.444-296T>G	XP_011531372.1:n.444-296T>G
XM_011533071.1:c.444-296T>G	XP_011531373.1:n.444-296T>G
XM_011533072.1:c.444-296T>G	XP_011531374.1:n.444-296T>G
XM_011533069.2:c.477-296T>G	XP_011531371.1:n.477-296T>G
XM_011533072.2:c.444-296T>G	XP_011531374.1:n.444-296T>G
NM_000348.4:c.699-296T>G MANE Select	NP_000339.2:n.699-296T>G