Canonical Allele Identifier: CA466130864

Gene: HSD17B3

Linked Data

• MyVariant Identifiers: chr9:g.99003172A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96240890A>G , CM000671.2:g.96240890A>G	GRCh38
NC_000009.11:g.99003172A>G , CM000671.1:g.99003172A>G	GRCh37
NC_000009.10:g.98042993A>G	NCBI36
NG_008157.1:g.66263T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000375262.4:c.672+3439T>C	ENSP00000364411.2:n.672+3439T>C
ENST00000375263.8:c.690T>C MANE Select	ENSP00000364412.3:p.Ala230=
ENST00000463517.2:n.2232T>C
ENST00000464104.6:n.1628T>C
ENST00000467499.6:c.*389T>C	ENSP00000498077.1:n.*389T>C
ENST00000484816.2:n.41T>C
ENST00000494814.6:n.240T>C
ENST00000643789.1:c.2982T>C
ENST00000648146.1:c.690T>C	ENSP00000497238.1:p.Ala230=
ENST00000648332.1:c.367T>C	ENSP00000497562.1:n.367T>C
ENST00000648799.1:c.582T>C	ENSP00000498039.1:p.Ala194=
ENST00000650005.1:c.619T>C	ENSP00000498121.1:n.619T>C
ENST00000375262.3:c.672+3439T>C	ENSP00000364411.2:n.672+3439T>C
ENST00000375263.7:c.690T>C	ENSP00000364412.3:p.Ala230=
ENST00000464104.5:n.543T>C
ENST00000484816.1:n.40T>C
ENST00000494814.5:n.249T>C
NM_000197.1:c.690T>C	NP_000188.1:p.Ala230=
XM_005251970.3:c.330T>C	XP_005252027.1:p.Ala110=
XM_011518618.1:c.690T>C	XP_011516920.1:p.Ala230=
XM_011518619.1:c.690T>C	XP_011516921.1:p.Ala230=
XM_011518620.1:c.582T>C	XP_011516922.1:p.Ala194=
XM_011518621.1:c.*11T>C	XP_011516923.1:n.*11T>C
NM_000197.2:c.690T>C MANE Select	NP_000188.1:p.Ala230=
XM_011518618.2:c.690T>C	XP_011516920.1:p.Ala230=
XM_011518619.2:c.690T>C	XP_011516921.1:p.Ala230=
XM_017014671.1:c.690T>C	XP_016870160.1:p.Ala230=
XM_017014672.1:c.690T>C	XP_016870161.1:p.Ala230=
XM_017014673.2:c.654T>C	XP_016870162.1:p.Ala218=
XM_017014674.1:c.582T>C	XP_016870163.1:p.Ala194=
XM_017014675.1:c.528T>C	XP_016870164.1:p.Ala176=
XM_017014677.1:c.330T>C	XP_016870166.1:p.Ala110=
XM_024447529.1:c.528T>C	XP_024303297.1:p.Ala176=
XR_002956778.1:n.3162T>C