Canonical Allele Identifier: CA2690771478
Gene: FBP1 HGNC NCBI

Linked Data

dbSNP Id: rs2131509546
gnomAD v4: 9-94639386-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94639386G>A , CM000671.2:g.94639386G>A GRCh38
NC_000009.11:g.97401668G>A , CM000671.1:g.97401668G>A GRCh37
NC_000009.10:g.96441489G>A NCBI36
NG_008174.1:g.5864C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375326.9:c.-76C>T MANE Select ENSP00000364475.5:n.-76C>T
ENST00000375326.8:c.-76C>T ENSP00000364475.4:n.-76C>T
ENST00000414122.1:c.-83+658C>T ENSP00000411619.1:n.-83+658C>T
ENST00000415431.5:c.-24-52C>T ENSP00000408025.1:n.-24-52C>T
NM_000507.3:c.-76C>T NP_000498.2:n.-76C>T
NM_001127628.1:c.-24-52C>T NP_001121100.1:n.-24-52C>T
XM_006717005.2:c.-77+658C>T XP_006717068.1:n.-77+658C>T
XM_006717005.4:c.-77+658C>T XP_006717068.1:n.-77+658C>T
NM_000507.4:c.-76C>T MANE Select NP_000498.2:n.-76C>T
NM_001127628.2:c.-24-52C>T NP_001121100.1:n.-24-52C>T