Canonical Allele Identifier: CA2634536808
Gene: HSD17B2 HGNC NCBI

Linked Data

gnomAD v4: 16-82095809-A-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.82095809A>T , CM000678.2:g.82095809A>T GRCh38
NC_000016.9:g.82129414A>T , CM000678.1:g.82129414A>T GRCh37
NC_000016.8:g.80686915A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000199936.9:c.803-2266A>T MANE Select ENSP00000199936.4:n.803-2266A>T
ENST00000199936.8:c.803-2266A>T ENSP00000199936.4:n.803-2266A>T
ENST00000566838.2:c.5200A>T ENSP00000456471.1:n.5200A>T
ENST00000568090.5:c.395-2266A>T ENSP00000456529.1:n.395-2266A>T
NM_002153.2:c.803-2266A>T NP_002144.1:n.803-2266A>T
XR_001751898.2:n.1021-2266A>T
NM_002153.3:c.803-2266A>T MANE Select NP_002144.1:n.803-2266A>T
Search 100 bp 5'
Search 100 bp 3'