Canonical Allele Identifier: CA724732267
Gene: HSD17B2 HGNC NCBI

Linked Data

dbSNP Id: rs1310890085

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000199936.9:c.803-2266A>G MANE Select ENSP00000199936.4:n.803-2266A>G
ENST00000199936.8:c.803-2266A>G ENSP00000199936.4:n.803-2266A>G
ENST00000566838.2:c.5200A>G ENSP00000456471.1:n.5200A>G
ENST00000568090.5:c.395-2266A>G ENSP00000456529.1:n.395-2266A>G
NM_002153.2:c.803-2266A>G NP_002144.1:n.803-2266A>G
XR_001751898.2:n.1021-2266A>G
NM_002153.3:c.803-2266A>G MANE Select NP_002144.1:n.803-2266A>G