Canonical Allele Identifier: CA285228192
Gene: HSD17B2 HGNC NCBI

Linked Data

dbSNP Id: rs1424151

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.82095747A>G , CM000678.2:g.82095747A>G GRCh38
NC_000016.9:g.82129352A>G , CM000678.1:g.82129352A>G GRCh37
NC_000016.8:g.80686853A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000199936.9:c.803-2328A>G MANE Select ENSP00000199936.4:n.803-2328A>G
ENST00000199936.8:c.803-2328A>G ENSP00000199936.4:n.803-2328A>G
ENST00000566838.2:c.5138A>G ENSP00000456471.1:n.5138A>G
ENST00000568090.5:c.395-2328A>G ENSP00000456529.1:n.395-2328A>G
NM_002153.2:c.803-2328A>G NP_002144.1:n.803-2328A>G
XR_001751898.2:n.1021-2328A>G
NM_002153.3:c.803-2328A>G MANE Select NP_002144.1:n.803-2328A>G