Canonical Allele Identifier: CA1141187978

Gene: HSD3B2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119422246C= , CM000663.2:g.119422246C=	GRCh38
NC_000001.10:g.119964869C= , CM000663.1:g.119964869C=	GRCh37
NC_000001.9:g.119766392C=	NCBI36
NG_013349.1:g.12316C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000369416.4:c.745C= MANE Select	ENSP00000358424.3:p.Arg249=
ENST00000369416.3:c.745C=	ENSP00000358424.3:p.Arg249=
ENST00000543831.5:c.745C=	ENSP00000445122.1:p.Arg249=
NM_000198.3:c.745C=	NP_000189.1:p.Arg249=
NM_001166120.1:c.745C=	NP_001159592.1:p.Arg249=
NM_000198.4:c.745C= MANE Select	NP_000189.1:p.Arg249=
NM_001166120.2:c.745C=	NP_001159592.1:p.Arg249=