Canonical Allele Identifier: CA724732206

Gene: HSD17B2

Linked Data

• dbSNP Id: rs1452909943
• MyVariant Identifiers: chr16:g.82129290G>T (hg19) ; chr16:g.82095685G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.82095685G>T , CM000678.2:g.82095685G>T	GRCh38
NC_000016.9:g.82129290G>T , CM000678.1:g.82129290G>T	GRCh37
NC_000016.8:g.80686791G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000199936.9:c.803-2390G>T MANE Select	ENSP00000199936.4:n.803-2390G>T
ENST00000199936.8:c.803-2390G>T	ENSP00000199936.4:n.803-2390G>T
ENST00000566838.2:c.5076G>T	ENSP00000456471.1:n.5076G>T
ENST00000568090.5:c.395-2390G>T	ENSP00000456529.1:n.395-2390G>T
NM_002153.2:c.803-2390G>T	NP_002144.1:n.803-2390G>T
XR_001751898.2:n.1021-2390G>T
NM_002153.3:c.803-2390G>T MANE Select	NP_002144.1:n.803-2390G>T