Canonical Allele Identifier: CA1192292353

Gene: HSD3B2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119421878A= , CM000663.2:g.119421878A=	GRCh38
NC_000001.10:g.119964501A= , CM000663.1:g.119964501A=	GRCh37
NC_000001.9:g.119766024A=	NCBI36
NG_013349.1:g.11948A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369416.4:c.377A= MANE Select	ENSP00000358424.3:p.Glu126=
ENST00000369416.3:c.377A=	ENSP00000358424.3:p.Glu126=
ENST00000433745.5:c.377A=	ENSP00000388292.1:p.Glu126=
ENST00000448448.2:n.321A=
ENST00000543831.5:c.377A=	ENSP00000445122.1:p.Glu126=
NM_000198.3:c.377A=	NP_000189.1:p.Glu126=
NM_001166120.1:c.377A=	NP_001159592.1:p.Glu126=
NM_000198.4:c.377A= MANE Select	NP_000189.1:p.Glu126=
NM_001166120.2:c.377A=	NP_001159592.1:p.Glu126=