Canonical Allele Identifier: CA466130183

Gene: HSD17B3

Linked Data

• MyVariant Identifiers: chr9:g.98998183G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96235901G>A , CM000671.2:g.96235901G>A	GRCh38
NC_000009.11:g.98998183G>A , CM000671.1:g.98998183G>A	GRCh37
NC_000009.10:g.98038004G>A	NCBI36
NG_008157.1:g.71252C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375262.4:c.673-331C>T	ENSP00000364411.2:n.673-331C>T
ENST00000375263.8:c.823-331C>T MANE Select	ENSP00000364412.3:n.823-331C>T
ENST00000463517.2:n.2365-331C>T
ENST00000464104.6:n.1761-331C>T
ENST00000467499.6:c.*522-331C>T	ENSP00000498077.1:n.*522-331C>T
ENST00000494814.6:n.373-331C>T
ENST00000643789.1:c.3115-331C>T
ENST00000648146.1:c.961-331C>T	ENSP00000497238.1:n.961-331C>T
ENST00000648332.1:c.500-331C>T	ENSP00000497562.1:n.500-331C>T
ENST00000648799.1:c.715-331C>T	ENSP00000498039.1:n.715-331C>T
ENST00000650005.1:c.752-331C>T	ENSP00000498121.1:n.752-331C>T
ENST00000375262.3:c.673-331C>T	ENSP00000364411.2:n.673-331C>T
ENST00000375263.7:c.823-331C>T	ENSP00000364412.3:n.823-331C>T
ENST00000464104.5:n.676-331C>T
ENST00000467499.5:n.83-331C>T
ENST00000494814.5:n.382-331C>T
NM_000197.1:c.823-331C>T	NP_000188.1:n.823-331C>T
XM_005251970.3:c.463-331C>T	XP_005252027.1:n.463-331C>T
XM_011518618.1:c.823-331C>T	XP_011516920.1:n.823-331C>T
XM_011518619.1:c.823-331C>T	XP_011516921.1:n.823-331C>T
XM_011518620.1:c.715-331C>T	XP_011516922.1:n.715-331C>T
NM_000197.2:c.823-331C>T MANE Select	NP_000188.1:n.823-331C>T
XM_011518618.2:c.823-331C>T	XP_011516920.1:n.823-331C>T
XM_011518619.2:c.823-331C>T	XP_011516921.1:n.823-331C>T
XM_017014671.1:c.823-331C>T	XP_016870160.1:n.823-331C>T
XM_017014672.1:c.823-331C>T	XP_016870161.1:n.823-331C>T
XM_017014673.2:c.787-331C>T	XP_016870162.1:n.787-331C>T
XM_017014674.1:c.715-331C>T	XP_016870163.1:n.715-331C>T
XM_017014675.1:c.661-331C>T	XP_016870164.1:n.661-331C>T
XM_017014677.1:c.463-331C>T	XP_016870166.1:n.463-331C>T
XM_024447529.1:c.661-331C>T	XP_024303297.1:n.661-331C>T
XR_002956778.1:n.3295-331C>T