Canonical Allele Identifier: CA1192293672

Gene: HSD3B2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119422839C= , CM000663.2:g.119422839C=	GRCh38
NC_000001.10:g.119965462C= , CM000663.1:g.119965462C=	GRCh37
NC_000001.9:g.119766985C=	NCBI36
NG_013349.1:g.12909C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000369416.4:c.*219C= MANE Select	ENSP00000358424.3:n.*219C=
ENST00000369416.3:c.*219C=	ENSP00000358424.3:n.*219C=
ENST00000543831.5:c.*219C=	ENSP00000445122.1:n.*219C=
NM_000198.3:c.*219C=	NP_000189.1:n.*219C=
NM_001166120.1:c.*219C=	NP_001159592.1:n.*219C=
NM_000198.4:c.*219C= MANE Select	NP_000189.1:n.*219C=
NM_001166120.2:c.*219C=	NP_001159592.1:n.*219C=