Canonical Allele Identifier: CA466129440

Gene: HSD17B3

Linked Data

• gnomAD v4: 9-96235412-G-T
• MyVariant Identifiers: chr9:g.98997694G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96235412G>T , CM000671.2:g.96235412G>T	GRCh38
NC_000009.11:g.98997694G>T , CM000671.1:g.98997694G>T	GRCh37
NC_000009.10:g.98037515G>T	NCBI36
NG_008157.1:g.71741C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375263.8:c.*48C>A MANE Select	ENSP00000364412.3:n.*48C>A
ENST00000463517.2:n.2523C>A
ENST00000464104.6:n.1919C>A
ENST00000467499.6:c.*680C>A	ENSP00000498077.1:n.*680C>A
ENST00000494814.6:n.531C>A
ENST00000643789.1:c.3273C>A
ENST00000375262.3:c.*48C>A	ENSP00000364411.2:n.*48C>A
ENST00000375263.7:c.*48C>A	ENSP00000364412.3:n.*48C>A
ENST00000464104.5:n.834C>A
ENST00000467499.5:n.241C>A
ENST00000494814.5:n.540C>A
NM_000197.1:c.*48C>A	NP_000188.1:n.*48C>A
XM_005251970.3:c.*48C>A	XP_005252027.1:n.*48C>A
XM_011518618.1:c.*48C>A	XP_011516920.1:n.*48C>A
XM_011518619.1:c.*48C>A	XP_011516921.1:n.*48C>A
XM_011518620.1:c.*48C>A	XP_011516922.1:n.*48C>A
NM_000197.2:c.*48C>A MANE Select	NP_000188.1:n.*48C>A
XM_011518618.2:c.*48C>A	XP_011516920.1:n.*48C>A
XM_011518619.2:c.*48C>A	XP_011516921.1:n.*48C>A
XM_017014671.1:c.*48C>A	XP_016870160.1:n.*48C>A
XM_017014672.1:c.*48C>A	XP_016870161.1:n.*48C>A
XM_017014673.2:c.*48C>A	XP_016870162.1:n.*48C>A
XM_017014674.1:c.*48C>A	XP_016870163.1:n.*48C>A
XM_017014675.1:c.*48C>A	XP_016870164.1:n.*48C>A
XM_017014677.1:c.*48C>A	XP_016870166.1:n.*48C>A
XM_024447529.1:c.*48C>A	XP_024303297.1:n.*48C>A
XR_002956778.1:n.3453C>A