Canonical Allele Identifier: CA589584192

Gene: FBP1

Linked Data

• dbSNP Id: rs1369941106
• gnomAD v2: 9-97401674-A-G
• gnomAD v3: 9-94639392-A-G
• gnomAD v4: 9-94639392-A-G
• MyVariant Identifiers: chr9:g.97401674A>G (hg19) ; chr9:g.94639392A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94639392A>G , CM000671.2:g.94639392A>G	GRCh38
NC_000009.11:g.97401674A>G , CM000671.1:g.97401674A>G	GRCh37
NC_000009.10:g.96441495A>G	NCBI36
NG_008174.1:g.5858T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375326.9:c.-82T>C MANE Select	ENSP00000364475.5:n.-82T>C
ENST00000375326.8:c.-82T>C	ENSP00000364475.4:n.-82T>C
ENST00000414122.1:c.-83+652T>C	ENSP00000411619.1:n.-83+652T>C
ENST00000415431.5:c.-24-58T>C	ENSP00000408025.1:n.-24-58T>C
NM_000507.3:c.-82T>C	NP_000498.2:n.-82T>C
NM_001127628.1:c.-24-58T>C	NP_001121100.1:n.-24-58T>C
XM_006717005.2:c.-77+652T>C	XP_006717068.1:n.-77+652T>C
XM_006717005.4:c.-77+652T>C	XP_006717068.1:n.-77+652T>C
NM_000507.4:c.-82T>C MANE Select	NP_000498.2:n.-82T>C
NM_001127628.2:c.-24-58T>C	NP_001121100.1:n.-24-58T>C