Canonical Allele Identifier: CA2697557880

Gene: FBP1

Linked Data

• ClinVar Variation Id: 2699920
• ClinVar RCV Id: RCV003496082

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94609906T>C , CM000671.2:g.94609906T>C	GRCh38
NC_000009.11:g.97372188T>C , CM000671.1:g.97372188T>C	GRCh37
NC_000009.10:g.96412009T>C	NCBI36
NG_008174.1:g.35344A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682520.1:c.567+15A>G	ENSP00000507547.1:n.567+15A>G
ENST00000375326.9:c.567+15A>G MANE Select	ENSP00000364475.5:n.567+15A>G
ENST00000648117.1:c.372+15A>G	ENSP00000498145.1:n.372+15A>G
ENST00000375326.8:c.567+15A>G	ENSP00000364475.4:n.567+15A>G
ENST00000414122.1:c.315+15A>G	ENSP00000411619.1:n.315+15A>G
ENST00000415431.5:c.567+15A>G	ENSP00000408025.1:n.567+15A>G
NM_000507.3:c.567+15A>G	NP_000498.2:n.567+15A>G
NM_001127628.1:c.567+15A>G	NP_001121100.1:n.567+15A>G
XM_006717005.2:c.321+15A>G	XP_006717068.1:n.321+15A>G
XM_006717005.4:c.321+15A>G	XP_006717068.1:n.321+15A>G
NM_000507.4:c.567+15A>G MANE Select	NP_000498.2:n.567+15A>G
NM_001127628.2:c.567+15A>G	NP_001121100.1:n.567+15A>G