Canonical Allele Identifier: CA466099571

Gene: FBP1

Linked Data

• MyVariant Identifiers: chr9:g.97367742T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94605460T>G , CM000671.2:g.94605460T>G	GRCh38
NC_000009.11:g.97367742T>G , CM000671.1:g.97367742T>G	GRCh37
NC_000009.10:g.96407563T>G	NCBI36
NG_008174.1:g.39790A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682520.1:c.982A>C	ENSP00000507547.1:n.982A>C
ENST00000375326.9:c.822A>C MANE Select	ENSP00000364475.5:p.Gly274=
ENST00000648117.1:c.627A>C	ENSP00000498145.1:p.Gly209=
ENST00000375326.8:c.822A>C	ENSP00000364475.4:p.Gly274=
ENST00000415431.5:c.822A>C	ENSP00000408025.1:p.Gly274=
NM_000507.3:c.822A>C	NP_000498.2:p.Gly274=
NM_001127628.1:c.822A>C	NP_001121100.1:p.Gly274=
XM_006717005.2:c.576A>C	XP_006717068.1:p.Gly192=
XM_006717005.4:c.576A>C	XP_006717068.1:p.Gly192=
NM_000507.4:c.822A>C MANE Select	NP_000498.2:p.Gly274=
NM_001127628.2:c.822A>C	NP_001121100.1:p.Gly274=