Canonical Allele Identifier: CA346598437

Gene: SRD5A2

Linked Data

• dbSNP Id: rs780448796
• gnomAD v3: 2-31533620-T-C
• gnomAD v4: 2-31533620-T-C
• MyVariant Identifiers: chr2:g.31758690T>C (hg19) ; chr2:g.31533620T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31533620T>C , CM000664.2:g.31533620T>C	GRCh38
NC_000002.11:g.31758690T>C , CM000664.1:g.31758690T>C	GRCh37
NC_000002.10:g.31612194T>C	NCBI36
NG_008365.1:g.52352A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.428A>G MANE Select	ENSP00000477587.1:p.Asp143Gly
ENST00000622030.1:c.428A>G	ENSP00000477587.1:p.Asp143Gly
NM_000348.3:c.428A>G	NP_000339.2:p.Asp143Gly
XM_011533068.1:c.428A>G	XP_011531370.1:p.Asp143Gly
XM_011533069.1:c.206A>G	XP_011531371.1:p.Asp69Gly
XM_011533070.1:c.173A>G	XP_011531372.1:p.Asp58Gly
XM_011533071.1:c.173A>G	XP_011531373.1:p.Asp58Gly
XM_011533072.1:c.173A>G	XP_011531374.1:p.Asp58Gly
XM_011533069.2:c.206A>G	XP_011531371.1:p.Asp69Gly
XM_011533072.2:c.173A>G	XP_011531374.1:p.Asp58Gly
NM_000348.4:c.428A>G MANE Select	NP_000339.2:p.Asp143Gly