Canonical Allele Identifier: CA2690771537
Gene: FBP1 HGNC NCBI

Linked Data

gnomAD v4: 9-94639441-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94639441C>A , CM000671.2:g.94639441C>A GRCh38
NC_000009.11:g.97401723C>A , CM000671.1:g.97401723C>A GRCh37
NC_000009.10:g.96441544C>A NCBI36
NG_008174.1:g.5809G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375326.9:c.-131G>T MANE Select ENSP00000364475.5:n.-131G>T
ENST00000375326.8:c.-131G>T ENSP00000364475.4:n.-131G>T
ENST00000414122.1:c.-83+603G>T ENSP00000411619.1:n.-83+603G>T
ENST00000415431.5:c.-24-107G>T ENSP00000408025.1:n.-24-107G>T
NM_000507.3:c.-131G>T NP_000498.2:n.-131G>T
NM_001127628.1:c.-24-107G>T NP_001121100.1:n.-24-107G>T
XM_006717005.2:c.-77+603G>T XP_006717068.1:n.-77+603G>T
XM_006717005.4:c.-77+603G>T XP_006717068.1:n.-77+603G>T
NM_000507.4:c.-131G>T MANE Select NP_000498.2:n.-131G>T
NM_001127628.2:c.-24-107G>T NP_001121100.1:n.-24-107G>T