Canonical Allele Identifier: CA1126949924
Gene: FBP1 HGNC NCBI

Linked Data

dbSNP Id: rs1828250757
gnomAD v3: 9-94639380-A-C
gnomAD v4: 9-94639380-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94639380A>C , CM000671.2:g.94639380A>C GRCh38
NC_000009.11:g.97401662A>C , CM000671.1:g.97401662A>C GRCh37
NC_000009.10:g.96441483A>C NCBI36
NG_008174.1:g.5870T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375326.9:c.-70T>G MANE Select ENSP00000364475.5:n.-70T>G
ENST00000375326.8:c.-70T>G ENSP00000364475.4:n.-70T>G
ENST00000414122.1:c.-83+664T>G ENSP00000411619.1:n.-83+664T>G
ENST00000415431.5:c.-24-46T>G ENSP00000408025.1:n.-24-46T>G
NM_000507.3:c.-70T>G NP_000498.2:n.-70T>G
NM_001127628.1:c.-24-46T>G NP_001121100.1:n.-24-46T>G
XM_006717005.2:c.-77+664T>G XP_006717068.1:n.-77+664T>G
XM_006717005.4:c.-77+664T>G XP_006717068.1:n.-77+664T>G
NM_000507.4:c.-70T>G MANE Select NP_000498.2:n.-70T>G
NM_001127628.2:c.-24-46T>G NP_001121100.1:n.-24-46T>G