Canonical Allele Identifier: CA285228143

Gene: HSD17B2

Linked Data

• dbSNP Id: rs767462921
• MyVariant Identifiers: chr16:g.82129277C>G (hg19) ; chr16:g.82095672C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.82095672C>G , CM000678.2:g.82095672C>G	GRCh38
NC_000016.9:g.82129277C>G , CM000678.1:g.82129277C>G	GRCh37
NC_000016.8:g.80686778C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000199936.9:c.803-2403C>G MANE Select	ENSP00000199936.4:n.803-2403C>G
ENST00000199936.8:c.803-2403C>G	ENSP00000199936.4:n.803-2403C>G
ENST00000566838.2:c.5063C>G	ENSP00000456471.1:n.5063C>G
ENST00000568090.5:c.395-2403C>G	ENSP00000456529.1:n.395-2403C>G
NM_002153.2:c.803-2403C>G	NP_002144.1:n.803-2403C>G
XR_001751898.2:n.1021-2403C>G
NM_002153.3:c.803-2403C>G MANE Select	NP_002144.1:n.803-2403C>G