Canonical Allele Identifier: CA1865981450
Gene: HSD17B3 HGNC NCBI

Linked Data

dbSNP Id: rs1836360899

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.96239756G>C , CM000671.2:g.96239756G>C GRCh38
NC_000009.11:g.99002038G>C , CM000671.1:g.99002038G>C GRCh37
NC_000009.10:g.98041859G>C NCBI36
NG_008157.1:g.67397C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375262.4:c.673-4186C>G ENSP00000364411.2:n.673-4186C>G
ENST00000375263.8:c.822+1002C>G MANE Select ENSP00000364412.3:n.822+1002C>G
ENST00000463517.2:n.2364+1002C>G
ENST00000464104.6:n.1760+1002C>G
ENST00000467499.6:c.*521+1002C>G ENSP00000498077.1:n.*521+1002C>G
ENST00000484816.2:n.174-85C>G
ENST00000494814.6:n.372+1002C>G
ENST00000643789.1:c.3114+1002C>G
ENST00000648146.1:c.960+67C>G ENSP00000497238.1:n.960+67C>G
ENST00000648332.1:c.499+1002C>G ENSP00000497562.1:n.499+1002C>G
ENST00000648799.1:c.714+1002C>G ENSP00000498039.1:n.714+1002C>G
ENST00000650005.1:c.751+1002C>G ENSP00000498121.1:n.751+1002C>G
ENST00000375262.3:c.673-4186C>G ENSP00000364411.2:n.673-4186C>G
ENST00000375263.7:c.822+1002C>G ENSP00000364412.3:n.822+1002C>G
ENST00000464104.5:n.675+1002C>G
ENST00000467499.5:n.82+67C>G
ENST00000484816.1:n.173-85C>G
ENST00000494814.5:n.381+1002C>G
NM_000197.1:c.822+1002C>G NP_000188.1:n.822+1002C>G
XM_005251970.3:c.462+1002C>G XP_005252027.1:n.462+1002C>G
XM_011518618.1:c.822+1002C>G XP_011516920.1:n.822+1002C>G
XM_011518619.1:c.822+1002C>G XP_011516921.1:n.822+1002C>G
XM_011518620.1:c.714+1002C>G XP_011516922.1:n.714+1002C>G
NM_000197.2:c.822+1002C>G MANE Select NP_000188.1:n.822+1002C>G
XM_011518618.2:c.822+1002C>G XP_011516920.1:n.822+1002C>G
XM_011518619.2:c.822+1002C>G XP_011516921.1:n.822+1002C>G
XM_017014671.1:c.822+1002C>G XP_016870160.1:n.822+1002C>G
XM_017014672.1:c.822+1002C>G XP_016870161.1:n.822+1002C>G
XM_017014673.2:c.786+1002C>G XP_016870162.1:n.786+1002C>G
XM_017014674.1:c.714+1002C>G XP_016870163.1:n.714+1002C>G
XM_017014675.1:c.660+1002C>G XP_016870164.1:n.660+1002C>G
XM_017014677.1:c.462+1002C>G XP_016870166.1:n.462+1002C>G
XM_024447529.1:c.660+1002C>G XP_024303297.1:n.660+1002C>G
XR_002956778.1:n.3294+1002C>G