Canonical Allele Identifier: CA1192292508

Gene: HSD3B2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119422026T= , CM000663.2:g.119422026T=	GRCh38
NC_000001.10:g.119964649T= , CM000663.1:g.119964649T=	GRCh37
NC_000001.9:g.119766172T=	NCBI36
NG_013349.1:g.12096T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000369416.4:c.525T= MANE Select	ENSP00000358424.3:p.Asn175=
ENST00000369416.3:c.525T=	ENSP00000358424.3:p.Asn175=
ENST00000433745.5:c.525T=	ENSP00000388292.1:p.Asn175=
ENST00000543831.5:c.525T=	ENSP00000445122.1:p.Asn175=
NM_000198.3:c.525T=	NP_000189.1:p.Asn175=
NM_001166120.1:c.525T=	NP_001159592.1:p.Asn175=
NM_000198.4:c.525T= MANE Select	NP_000189.1:p.Asn175=
NM_001166120.2:c.525T=	NP_001159592.1:p.Asn175=