Canonical Allele Identifier: CA466132149

Gene: HSD17B3

Linked Data

• MyVariant Identifiers: chr9:g.99006620G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96244338G>C , CM000671.2:g.96244338G>C	GRCh38
NC_000009.11:g.99006620G>C , CM000671.1:g.99006620G>C	GRCh37
NC_000009.10:g.98046441G>C	NCBI36
NG_008157.1:g.62815C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375262.4:c.663C>G	ENSP00000364411.2:p.Val221=
ENST00000375263.8:c.663C>G MANE Select	ENSP00000364412.3:p.Val221=
ENST00000463517.2:n.2205C>G
ENST00000464104.6:n.1601C>G
ENST00000467499.6:c.*362C>G	ENSP00000498077.1:n.*362C>G
ENST00000484816.2:n.14C>G
ENST00000494814.6:n.175C>G
ENST00000643789.1:c.2955C>G
ENST00000648146.1:c.663C>G	ENSP00000497238.1:p.Val221=
ENST00000648332.1:c.340C>G	ENSP00000497562.1:n.340C>G
ENST00000648799.1:c.555C>G	ENSP00000498039.1:p.Val185=
ENST00000650005.1:c.592C>G	ENSP00000498121.1:n.592C>G
ENST00000375262.3:c.663C>G	ENSP00000364411.2:p.Val221=
ENST00000375263.7:c.663C>G	ENSP00000364412.3:p.Val221=
ENST00000464104.5:n.516C>G
ENST00000484816.1:n.13C>G
ENST00000494814.5:n.184C>G
NM_000197.1:c.663C>G	NP_000188.1:p.Val221=
XM_005251970.3:c.303C>G	XP_005252027.1:p.Val101=
XM_011518618.1:c.663C>G	XP_011516920.1:p.Val221=
XM_011518619.1:c.663C>G	XP_011516921.1:p.Val221=
XM_011518620.1:c.555C>G	XP_011516922.1:p.Val185=
XM_011518621.1:c.663C>G	XP_011516923.1:p.Val221=
NM_000197.2:c.663C>G MANE Select	NP_000188.1:p.Val221=
XM_011518618.2:c.663C>G	XP_011516920.1:p.Val221=
XM_011518619.2:c.663C>G	XP_011516921.1:p.Val221=
XM_017014671.1:c.663C>G	XP_016870160.1:p.Val221=
XM_017014672.1:c.663C>G	XP_016870161.1:p.Val221=
XM_017014673.2:c.627C>G	XP_016870162.1:p.Val209=
XM_017014674.1:c.555C>G	XP_016870163.1:p.Val185=
XM_017014675.1:c.501C>G	XP_016870164.1:p.Val167=
XM_017014677.1:c.303C>G	XP_016870166.1:p.Val101=
XM_024447529.1:c.501C>G	XP_024303297.1:p.Val167=
XR_002956778.1:n.3097C>G