Canonical Allele Identifier: CA1139993720

Gene: HSD3B1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119508823G= , CM000663.2:g.119508823G=	GRCh38
NC_000001.10:g.120051446G= , CM000663.1:g.120051446G=	GRCh37
NC_000001.9:g.119852969G=	NCBI36
NG_050909.1:g.6712G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369413.8:c.145+1202G= MANE Select	ENSP00000358421.3:n.145+1202G=
ENST00000369413.7:c.145+1202G=	ENSP00000358421.3:n.145+1202G=
ENST00000492140.1:n.280+1202G=
ENST00000528909.1:c.145+1202G=	ENSP00000432268.1:n.145+1202G=
ENST00000531340.5:c.145+1202G=	ENSP00000435999.1:n.145+1202G=
NM_000862.2:c.145+1202G=	NP_000853.1:n.145+1202G=
XM_011541314.1:c.151+1202G=	XP_011539616.1:n.151+1202G=
NM_001328615.1:c.145+1202G=	NP_001315544.1:n.145+1202G=
NM_000862.3:c.145+1202G= MANE Select	NP_000853.1:n.145+1202G=