Canonical Allele Identifier: CA466099852

Gene: FBP1

Linked Data

• MyVariant Identifiers: chr9:g.97367838C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94605556C>A , CM000671.2:g.94605556C>A	GRCh38
NC_000009.11:g.97367838C>A , CM000671.1:g.97367838C>A	GRCh37
NC_000009.10:g.96407659C>A	NCBI36
NG_008174.1:g.39694G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682520.1:c.886G>T	ENSP00000507547.1:n.886G>T
ENST00000375326.9:c.726G>T MANE Select	ENSP00000364475.5:p.Gly242=
ENST00000648117.1:c.531G>T	ENSP00000498145.1:p.Gly177=
ENST00000375326.8:c.726G>T	ENSP00000364475.4:p.Gly242=
ENST00000415431.5:c.726G>T	ENSP00000408025.1:p.Gly242=
NM_000507.3:c.726G>T	NP_000498.2:p.Gly242=
NM_001127628.1:c.726G>T	NP_001121100.1:p.Gly242=
XM_006717005.2:c.480G>T	XP_006717068.1:p.Gly160=
XM_006717005.4:c.480G>T	XP_006717068.1:p.Gly160=
NM_000507.4:c.726G>T MANE Select	NP_000498.2:p.Gly242=
NM_001127628.2:c.726G>T	NP_001121100.1:p.Gly242=