Canonical Allele Identifier: CA10634486

Gene: FBP1

Linked Data

• ClinVar Variation Id: 367562
• ClinVar RCV Id: RCV000271068
• dbSNP Id: rs28382860
• gnomAD v2: 9-97401746-G-C
• gnomAD v3: 9-94639464-G-C
• gnomAD v4: 9-94639464-G-C
• MyVariant Identifiers: chr9:g.97401746G>C (hg19) ; chr9:g.94639464G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94639464G>C , CM000671.2:g.94639464G>C	GRCh38
NC_000009.11:g.97401746G>C , CM000671.1:g.97401746G>C	GRCh37
NC_000009.10:g.96441567G>C	NCBI36
NG_008174.1:g.5786C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375326.9:c.-154C>G MANE Select	ENSP00000364475.5:n.-154C>G
ENST00000375326.8:c.-154C>G	ENSP00000364475.4:n.-154C>G
ENST00000414122.1:c.-83+580C>G	ENSP00000411619.1:n.-83+580C>G
ENST00000415431.5:c.-24-130C>G	ENSP00000408025.1:n.-24-130C>G
NM_000507.3:c.-154C>G	NP_000498.2:n.-154C>G
NM_001127628.1:c.-24-130C>G	NP_001121100.1:n.-24-130C>G
XM_006717005.2:c.-77+580C>G	XP_006717068.1:n.-77+580C>G
XM_006717005.4:c.-77+580C>G	XP_006717068.1:n.-77+580C>G
NM_000507.4:c.-154C>G MANE Select	NP_000498.2:n.-154C>G
NM_001127628.2:c.-24-130C>G	NP_001121100.1:n.-24-130C>G