Canonical Allele Identifier: CA1865227977

Gene: FBP1

Linked Data

• ClinVar Variation Id: 2786370
• ClinVar RCV Id: RCV003600636
• dbSNP Id: rs1301770177

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94609912G>T , CM000671.2:g.94609912G>T	GRCh38
NC_000009.11:g.97372194G>T , CM000671.1:g.97372194G>T	GRCh37
NC_000009.10:g.96412015G>T	NCBI36
NG_008174.1:g.35338C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682520.1:c.567+9C>A	ENSP00000507547.1:n.567+9C>A
ENST00000375326.9:c.567+9C>A MANE Select	ENSP00000364475.5:n.567+9C>A
ENST00000648117.1:c.372+9C>A	ENSP00000498145.1:n.372+9C>A
ENST00000375326.8:c.567+9C>A	ENSP00000364475.4:n.567+9C>A
ENST00000414122.1:c.315+9C>A	ENSP00000411619.1:n.315+9C>A
ENST00000415431.5:c.567+9C>A	ENSP00000408025.1:n.567+9C>A
NM_000507.3:c.567+9C>A	NP_000498.2:n.567+9C>A
NM_001127628.1:c.567+9C>A	NP_001121100.1:n.567+9C>A
XM_006717005.2:c.321+9C>A	XP_006717068.1:n.321+9C>A
XM_006717005.4:c.321+9C>A	XP_006717068.1:n.321+9C>A
NM_000507.4:c.567+9C>A MANE Select	NP_000498.2:n.567+9C>A
NM_001127628.2:c.567+9C>A	NP_001121100.1:n.567+9C>A