Canonical Allele Identifier: CA466100864

Gene: FBP1

Linked Data

• gnomAD v4: 9-94610002-T-C
• MyVariant Identifiers: chr9:g.97372284T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94610002T>C , CM000671.2:g.94610002T>C	GRCh38
NC_000009.11:g.97372284T>C , CM000671.1:g.97372284T>C	GRCh37
NC_000009.10:g.96412105T>C	NCBI36
NG_008174.1:g.35248A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682520.1:c.486A>G	ENSP00000507547.1:p.Ala162=
ENST00000375326.9:c.486A>G MANE Select	ENSP00000364475.5:p.Ala162=
ENST00000648117.1:c.291A>G	ENSP00000498145.1:p.Ala97=
ENST00000375326.8:c.486A>G	ENSP00000364475.4:p.Ala162=
ENST00000414122.1:c.234A>G	ENSP00000411619.1:p.Ala78=
ENST00000415431.5:c.486A>G	ENSP00000408025.1:p.Ala162=
NM_000507.3:c.486A>G	NP_000498.2:p.Ala162=
NM_001127628.1:c.486A>G	NP_001121100.1:p.Ala162=
XM_006717005.2:c.240A>G	XP_006717068.1:p.Ala80=
XM_006717005.4:c.240A>G	XP_006717068.1:p.Ala80=
NM_000507.4:c.486A>G MANE Select	NP_000498.2:p.Ala162=
NM_001127628.2:c.486A>G	NP_001121100.1:p.Ala162=