Canonical Allele Identifier: CA886224564

Gene: HSD3B2

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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