Canonical Allele Identifier: CA466102925

Gene: FBP1

Linked Data

• MyVariant Identifiers: chr9:g.97382686T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94620404T>C , CM000671.2:g.94620404T>C	GRCh38
NC_000009.11:g.97382686T>C , CM000671.1:g.97382686T>C	GRCh37
NC_000009.10:g.96422507T>C	NCBI36
NG_008174.1:g.24846A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682520.1:c.258A>G	ENSP00000507547.1:p.Leu86=
ENST00000375326.9:c.258A>G MANE Select	ENSP00000364475.5:p.Leu86=
ENST00000648117.1:c.156A>G	ENSP00000498145.1:p.Leu52=
ENST00000375326.8:c.258A>G	ENSP00000364475.4:p.Leu86=
ENST00000414122.1:c.6A>G	ENSP00000411619.1:p.Leu2=
ENST00000415431.5:c.258A>G	ENSP00000408025.1:p.Leu86=
NM_000507.3:c.258A>G	NP_000498.2:p.Leu86=
NM_001127628.1:c.258A>G	NP_001121100.1:p.Leu86=
XM_006717005.2:c.12A>G	XP_006717068.1:p.Leu4=
XM_006717005.4:c.12A>G	XP_006717068.1:p.Leu4=
NM_000507.4:c.258A>G MANE Select	NP_000498.2:p.Leu86=
NM_001127628.2:c.258A>G	NP_001121100.1:p.Leu86=