Canonical Allele Identifier: CA531714050

Gene: SRD5A2

Linked Data

• dbSNP Id: rs1412696768
• gnomAD v2: 2-31763575-A-C
• gnomAD v3: 2-31538505-A-C
• gnomAD v4: 2-31538505-A-C
• MyVariant Identifiers: chr2:g.31763575A>C (hg19) ; chr2:g.31538505A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31538505A>C , CM000664.2:g.31538505A>C	GRCh38
NC_000002.11:g.31763575A>C , CM000664.1:g.31763575A>C	GRCh37
NC_000002.10:g.31617079A>C	NCBI36
NG_008365.1:g.47467T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000622030.2:c.282-4739T>G MANE Select	ENSP00000477587.1:n.282-4739T>G
ENST00000622030.1:c.282-4739T>G	ENSP00000477587.1:n.282-4739T>G
NM_000348.3:c.282-4739T>G	NP_000339.2:n.282-4739T>G
XM_011533068.1:c.282-4739T>G	XP_011531370.1:n.282-4739T>G
XM_011533069.1:c.60-4739T>G	XP_011531371.1:n.60-4739T>G
XM_011533070.1:c.27-4739T>G	XP_011531372.1:n.27-4739T>G
XM_011533071.1:c.27-4739T>G	XP_011531373.1:n.27-4739T>G
XM_011533072.1:c.27-4739T>G	XP_011531374.1:n.27-4739T>G
XM_011533069.2:c.60-4739T>G	XP_011531371.1:n.60-4739T>G
XM_011533072.2:c.27-4739T>G	XP_011531374.1:n.27-4739T>G
NM_000348.4:c.282-4739T>G MANE Select	NP_000339.2:n.282-4739T>G