Canonical Allele Identifier: CA531723356

Gene: SRD5A2

Linked Data

• dbSNP Id: rs1346715826
• gnomAD v2: 2-31805568-G-C
• gnomAD v3: 2-31580498-G-C
• gnomAD v4: 2-31580498-G-C
• MyVariant Identifiers: chr2:g.31805568G>C (hg19) ; chr2:g.31580498G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31580498G>C , CM000664.2:g.31580498G>C	GRCh38
NC_000002.11:g.31805568G>C , CM000664.1:g.31805568G>C	GRCh37
NC_000002.10:g.31659072G>C	NCBI36
NG_008365.1:g.5474C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.281+122C>G MANE Select	ENSP00000477587.1:n.281+122C>G
ENST00000622030.1:c.281+122C>G	ENSP00000477587.1:n.281+122C>G
NM_000348.3:c.281+122C>G	NP_000339.2:n.281+122C>G
XM_011533068.1:c.281+122C>G	XP_011531370.1:n.281+122C>G
XM_011533070.1:c.27-46732C>G	XP_011531372.1:n.27-46732C>G
XM_011533071.1:c.27-46732C>G	XP_011531373.1:n.27-46732C>G
XM_011533072.1:c.27-46732C>G	XP_011531374.1:n.27-46732C>G
XM_011533072.2:c.27-46732C>G	XP_011531374.1:n.27-46732C>G
NM_000348.4:c.281+122C>G MANE Select	NP_000339.2:n.281+122C>G