Canonical Allele Identifier: CA466265654

Gene: FBP1

Linked Data

• gnomAD v4: 9-94639146-C-G
• MyVariant Identifiers: chr9:g.97401428C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94639146C>G , CM000671.2:g.94639146C>G	GRCh38
NC_000009.11:g.97401428C>G , CM000671.1:g.97401428C>G	GRCh37
NC_000009.10:g.96441249C>G	NCBI36
NG_008174.1:g.6104G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682520.1:c.165G>C	ENSP00000507547.1:p.Ala55=
ENST00000375326.9:c.165G>C MANE Select	ENSP00000364475.5:p.Ala55=
ENST00000375326.8:c.165G>C	ENSP00000364475.4:p.Ala55=
ENST00000414122.1:c.-83+898G>C	ENSP00000411619.1:n.-83+898G>C
ENST00000415431.5:c.165G>C	ENSP00000408025.1:p.Ala55=
NM_000507.3:c.165G>C	NP_000498.2:p.Ala55=
NM_001127628.1:c.165G>C	NP_001121100.1:p.Ala55=
XM_006717005.2:c.-77+898G>C	XP_006717068.1:n.-77+898G>C
XM_006717005.4:c.-77+898G>C	XP_006717068.1:n.-77+898G>C
NM_000507.4:c.165G>C MANE Select	NP_000498.2:p.Ala55=
NM_001127628.2:c.165G>C	NP_001121100.1:p.Ala55=