Canonical Allele Identifier: CA346598450

Gene: SRD5A2

Linked Data

• MyVariant Identifiers: chr2:g.31758696T>G (hg19) ; chr2:g.31533626T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31533626T>G , CM000664.2:g.31533626T>G	GRCh38
NC_000002.11:g.31758696T>G , CM000664.1:g.31758696T>G	GRCh37
NC_000002.10:g.31612200T>G	NCBI36
NG_008365.1:g.52346A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.422A>C MANE Select	ENSP00000477587.1:p.Tyr141Ser
ENST00000622030.1:c.422A>C	ENSP00000477587.1:p.Tyr141Ser
NM_000348.3:c.422A>C	NP_000339.2:p.Tyr141Ser
XM_011533068.1:c.422A>C	XP_011531370.1:p.Tyr141Ser
XM_011533069.1:c.200A>C	XP_011531371.1:p.Tyr67Ser
XM_011533070.1:c.167A>C	XP_011531372.1:p.Tyr56Ser
XM_011533071.1:c.167A>C	XP_011531373.1:p.Tyr56Ser
XM_011533072.1:c.167A>C	XP_011531374.1:p.Tyr56Ser
XM_011533069.2:c.200A>C	XP_011531371.1:p.Tyr67Ser
XM_011533072.2:c.167A>C	XP_011531374.1:p.Tyr56Ser
NM_000348.4:c.422A>C MANE Select	NP_000339.2:p.Tyr141Ser