Canonical Allele Identifier: CA425568441

Gene: SRD5A2

Linked Data

• MyVariant Identifiers: chr2:g.31758791A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31533721A>C , CM000664.2:g.31533721A>C	GRCh38
NC_000002.11:g.31758791A>C , CM000664.1:g.31758791A>C	GRCh37
NC_000002.10:g.31612295A>C	NCBI36
NG_008365.1:g.52251T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.327T>G MANE Select	ENSP00000477587.1:p.Ala109=
ENST00000622030.1:c.327T>G	ENSP00000477587.1:p.Ala109=
NM_000348.3:c.327T>G	NP_000339.2:p.Ala109=
XM_011533068.1:c.327T>G	XP_011531370.1:p.Ala109=
XM_011533069.1:c.105T>G	XP_011531371.1:p.Ala35=
XM_011533070.1:c.72T>G	XP_011531372.1:p.Ala24=
XM_011533071.1:c.72T>G	XP_011531373.1:p.Ala24=
XM_011533072.1:c.72T>G	XP_011531374.1:p.Ala24=
XM_011533069.2:c.105T>G	XP_011531371.1:p.Ala35=
XM_011533072.2:c.72T>G	XP_011531374.1:p.Ala24=
NM_000348.4:c.327T>G MANE Select	NP_000339.2:p.Ala109=