Canonical Allele Identifier: CA374334978

Gene: FBP1

Linked Data

• gnomAD v4: 9-94639139-A-T
• MyVariant Identifiers: chr9:g.97401421A>T (hg19) ; chr9:g.94639139A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94639139A>T , CM000671.2:g.94639139A>T	GRCh38
NC_000009.11:g.97401421A>T , CM000671.1:g.97401421A>T	GRCh37
NC_000009.10:g.96441242A>T	NCBI36
NG_008174.1:g.6111T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682520.1:c.170+2T>A	ENSP00000507547.1:n.170+2T>A
ENST00000375326.9:c.170+2T>A MANE Select	ENSP00000364475.5:n.170+2T>A
ENST00000375326.8:c.170+2T>A	ENSP00000364475.4:n.170+2T>A
ENST00000414122.1:c.-83+905T>A	ENSP00000411619.1:n.-83+905T>A
ENST00000415431.5:c.170+2T>A	ENSP00000408025.1:n.170+2T>A
NM_000507.3:c.170+2T>A	NP_000498.2:n.170+2T>A
NM_001127628.1:c.170+2T>A	NP_001121100.1:n.170+2T>A
XM_006717005.2:c.-77+905T>A	XP_006717068.1:n.-77+905T>A
XM_006717005.4:c.-77+905T>A	XP_006717068.1:n.-77+905T>A
NM_000507.4:c.170+2T>A MANE Select	NP_000498.2:n.170+2T>A
NM_001127628.2:c.170+2T>A	NP_001121100.1:n.170+2T>A