Canonical Allele Identifier: CA1139969172

Gene: HSD3B2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119418756T= , CM000663.2:g.119418756T=	GRCh38
NC_000001.10:g.119961379T= , CM000663.1:g.119961379T=	GRCh37
NC_000001.9:g.119762902T=	NCBI36
NG_013349.1:g.8826T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000198.4:c.143-662T= MANE Select	NP_000189.1:n.143-662T=
ENST00000369416.4:c.143-662T= MANE Select	ENSP00000358424.3:n.143-662T=
NM_000198.3:c.143-662T=	NP_000189.1:n.143-662T=
NM_001166120.1:c.143-662T=	NP_001159592.1:n.143-662T=
NM_001166120.2:c.143-662T=	NP_001159592.1:n.143-662T=
ENST00000369416.3:c.143-662T=	ENSP00000358424.3:n.143-662T=
ENST00000433745.5:c.143-662T=	ENSP00000388292.1:n.143-662T=
ENST00000443865.2:n.403-662T=
ENST00000448448.2:n.87-662T=
ENST00000471656.5:n.284-662T=
ENST00000543831.5:c.143-662T=	ENSP00000445122.1:n.143-662T=