Canonical Allele Identifier: CA425567679

Gene: SRD5A2

Linked Data

• MyVariant Identifiers: chr2:g.31756529A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31531459A>G , CM000664.2:g.31531459A>G	GRCh38
NC_000002.11:g.31756529A>G , CM000664.1:g.31756529A>G	GRCh37
NC_000002.10:g.31610033A>G	NCBI36
NG_008365.1:g.54513T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.459T>C MANE Select	ENSP00000477587.1:p.Phe153=
ENST00000622030.1:c.459T>C	ENSP00000477587.1:p.Phe153=
NM_000348.3:c.459T>C	NP_000339.2:p.Phe153=
XM_011533069.1:c.237T>C	XP_011531371.1:p.Phe79=
XM_011533070.1:c.204T>C	XP_011531372.1:p.Phe68=
XM_011533071.1:c.204T>C	XP_011531373.1:p.Phe68=
XM_011533072.1:c.204T>C	XP_011531374.1:p.Phe68=
XM_011533069.2:c.237T>C	XP_011531371.1:p.Phe79=
XM_011533072.2:c.204T>C	XP_011531374.1:p.Phe68=
NM_000348.4:c.459T>C MANE Select	NP_000339.2:p.Phe153=