Canonical Allele Identifier: CA346598203

Gene: SRD5A2

Linked Data

• MyVariant Identifiers: chr2:g.31756462T>A (hg19) ; chr2:g.31531392T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31531392T>A , CM000664.2:g.31531392T>A	GRCh38
NC_000002.11:g.31756462T>A , CM000664.1:g.31756462T>A	GRCh37
NC_000002.10:g.31609966T>A	NCBI36
NG_008365.1:g.54580A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000622030.2:c.526A>T MANE Select	ENSP00000477587.1:p.Ile176Phe
ENST00000622030.1:c.526A>T	ENSP00000477587.1:p.Ile176Phe
NM_000348.3:c.526A>T	NP_000339.2:p.Ile176Phe
XM_011533069.1:c.304A>T	XP_011531371.1:p.Ile102Phe
XM_011533070.1:c.271A>T	XP_011531372.1:p.Ile91Phe
XM_011533071.1:c.271A>T	XP_011531373.1:p.Ile91Phe
XM_011533072.1:c.271A>T	XP_011531374.1:p.Ile91Phe
XM_011533069.2:c.304A>T	XP_011531371.1:p.Ile102Phe
XM_011533072.2:c.271A>T	XP_011531374.1:p.Ile91Phe
NM_000348.4:c.526A>T MANE Select	NP_000339.2:p.Ile176Phe