Canonical Allele Identifier: CA2634539024
Gene: HSD17B2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.82095575_82095576insAGC , CM000678.2:g.82095575_82095576insAGC GRCh38
NC_000016.9:g.82129180_82129181insAGC , CM000678.1:g.82129180_82129181insAGC GRCh37
NC_000016.8:g.80686681_80686682insAGC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000199936.9:c.803-2500_803-2499insAGC MANE Select ENSP00000199936.4:n.803-2500_803-2499insAGC
ENST00000199936.8:c.803-2500_803-2499insAGC ENSP00000199936.4:n.803-2500_803-2499insAGC
ENST00000566838.2:c.4966_4967insAGC ENSP00000456471.1:n.4966_4967insAGC
ENST00000568090.5:c.395-2500_395-2499insAGC ENSP00000456529.1:n.395-2500_395-2499insAGC
NM_002153.2:c.803-2500_803-2499insAGC NP_002144.1:n.803-2500_803-2499insAGC
XR_001751898.2:n.1021-2500_1021-2499insAGC
NM_002153.3:c.803-2500_803-2499insAGC MANE Select NP_002144.1:n.803-2500_803-2499insAGC