Canonical Allele Identifier: CA425567636

Gene: SRD5A2

Linked Data

• MyVariant Identifiers: chr2:g.31756511T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31531441T>A , CM000664.2:g.31531441T>A	GRCh38
NC_000002.11:g.31756511T>A , CM000664.1:g.31756511T>A	GRCh37
NC_000002.10:g.31610015T>A	NCBI36
NG_008365.1:g.54531A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.477A>T MANE Select	ENSP00000477587.1:p.Ile159=
ENST00000622030.1:c.477A>T	ENSP00000477587.1:p.Ile159=
NM_000348.3:c.477A>T	NP_000339.2:p.Ile159=
XM_011533069.1:c.255A>T	XP_011531371.1:p.Ile85=
XM_011533070.1:c.222A>T	XP_011531372.1:p.Ile74=
XM_011533071.1:c.222A>T	XP_011531373.1:p.Ile74=
XM_011533072.1:c.222A>T	XP_011531374.1:p.Ile74=
XM_011533069.2:c.255A>T	XP_011531371.1:p.Ile85=
XM_011533072.2:c.222A>T	XP_011531374.1:p.Ile74=
NM_000348.4:c.477A>T MANE Select	NP_000339.2:p.Ile159=