Canonical Allele Identifier: CA2634536811
Gene: HSD17B2 HGNC NCBI

Linked Data

gnomAD v4: 16-82095819-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.82095819C>A , CM000678.2:g.82095819C>A GRCh38
NC_000016.9:g.82129424C>A , CM000678.1:g.82129424C>A GRCh37
NC_000016.8:g.80686925C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000199936.9:c.803-2256C>A MANE Select ENSP00000199936.4:n.803-2256C>A
ENST00000199936.8:c.803-2256C>A ENSP00000199936.4:n.803-2256C>A
ENST00000566838.2:c.5210C>A ENSP00000456471.1:n.5210C>A
ENST00000568090.5:c.395-2256C>A ENSP00000456529.1:n.395-2256C>A
NM_002153.2:c.803-2256C>A NP_002144.1:n.803-2256C>A
XR_001751898.2:n.1021-2256C>A
NM_002153.3:c.803-2256C>A MANE Select NP_002144.1:n.803-2256C>A
Search 100 bp 5'
Search 100 bp 3'