Canonical Allele Identifier: CA466099587

Gene: FBP1

Linked Data

• gnomAD v4: 9-94605466-G-T
• MyVariant Identifiers: chr9:g.97367748G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94605466G>T , CM000671.2:g.94605466G>T	GRCh38
NC_000009.11:g.97367748G>T , CM000671.1:g.97367748G>T	GRCh37
NC_000009.10:g.96407569G>T	NCBI36
NG_008174.1:g.39784C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682520.1:c.976C>A	ENSP00000507547.1:n.976C>A
ENST00000375326.9:c.816C>A MANE Select	ENSP00000364475.5:p.Pro272=
ENST00000648117.1:c.621C>A	ENSP00000498145.1:p.Pro207=
ENST00000375326.8:c.816C>A	ENSP00000364475.4:p.Pro272=
ENST00000415431.5:c.816C>A	ENSP00000408025.1:p.Pro272=
NM_000507.3:c.816C>A	NP_000498.2:p.Pro272=
NM_001127628.1:c.816C>A	NP_001121100.1:p.Pro272=
XM_006717005.2:c.570C>A	XP_006717068.1:p.Pro190=
XM_006717005.4:c.570C>A	XP_006717068.1:p.Pro190=
NM_000507.4:c.816C>A MANE Select	NP_000498.2:p.Pro272=
NM_001127628.2:c.816C>A	NP_001121100.1:p.Pro272=