Canonical Allele Identifier: CA285245901
Gene: HSD17B2 HGNC NCBI
HSD17B2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs4243229

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.82051993A>G , CM000678.2:g.82051993A>G GRCh38
NC_000016.9:g.82085598A>G , CM000678.1:g.82085598A>G GRCh37
NC_000016.8:g.80643099A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000199936.9:c.266-16177A>G (HSD17B2) MANE Select ENSP00000199936.4:n.266-16177A>G
ENST00000199936.8:c.266-16177A>G (HSD17B2) ENSP00000199936.4:n.266-16177A>G
ENST00000563491.5:c.-143-16177A>G (HSD17B2) ENSP00000455992.1:n.-143-16177A>G
ENST00000566213.1:c.265+16304A>G (HSD17B2) ENSP00000457943.1:n.265+16304A>G
ENST00000569351.2:c.50-16177A>G (HSD17B2) ENSP00000454931.1:n.50-16177A>G
NM_002153.2:c.266-16177A>G (HSD17B2) NP_002144.1:n.266-16177A>G
XR_243405.2:n.454-16177A>G (HSD17B2)
XR_933796.1:n.1494+300T>C (HSD17B2-AS1)
XR_933797.1:n.1329-7385T>C (HSD17B2-AS1)
XR_001751898.2:n.415-16177A>G (HSD17B2)
XR_001752286.1:n.1530+300T>C (HSD17B2-AS1)
XR_933796.2:n.1530+300T>C (HSD17B2-AS1)
XR_933797.2:n.1365-7385T>C (HSD17B2-AS1)
NM_002153.3:c.266-16177A>G (HSD17B2) MANE Select NP_002144.1:n.266-16177A>G