Canonical Allele Identifier: CA346598666

Gene: SRD5A2

Linked Data

• MyVariant Identifiers: chr2:g.31758799A>C (hg19) ; chr2:g.31533729A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31533729A>C , CM000664.2:g.31533729A>C	GRCh38
NC_000002.11:g.31758799A>C , CM000664.1:g.31758799A>C	GRCh37
NC_000002.10:g.31612303A>C	NCBI36
NG_008365.1:g.52243T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.319T>G MANE Select	ENSP00000477587.1:p.Tyr107Asp
ENST00000622030.1:c.319T>G	ENSP00000477587.1:p.Tyr107Asp
NM_000348.3:c.319T>G	NP_000339.2:p.Tyr107Asp
XM_011533068.1:c.319T>G	XP_011531370.1:p.Tyr107Asp
XM_011533069.1:c.97T>G	XP_011531371.1:p.Tyr33Asp
XM_011533070.1:c.64T>G	XP_011531372.1:p.Tyr22Asp
XM_011533071.1:c.64T>G	XP_011531373.1:p.Tyr22Asp
XM_011533072.1:c.64T>G	XP_011531374.1:p.Tyr22Asp
XM_011533069.2:c.97T>G	XP_011531371.1:p.Tyr33Asp
XM_011533072.2:c.64T>G	XP_011531374.1:p.Tyr22Asp
NM_000348.4:c.319T>G MANE Select	NP_000339.2:p.Tyr107Asp