Canonical Allele Identifier: CA2579387350
Gene: FBP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94639330C>T , CM000671.2:g.94639330C>T GRCh38
NC_000009.11:g.97401612C>T , CM000671.1:g.97401612C>T GRCh37
NC_000009.10:g.96441433C>T NCBI36
NG_008174.1:g.5920G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375326.9:c.-20G>A MANE Select ENSP00000364475.5:n.-20G>A
ENST00000375326.8:c.-20G>A ENSP00000364475.4:n.-20G>A
ENST00000414122.1:c.-83+714G>A ENSP00000411619.1:n.-83+714G>A
ENST00000415431.5:c.-20G>A ENSP00000408025.1:n.-20G>A
NM_000507.3:c.-20G>A NP_000498.2:n.-20G>A
NM_001127628.1:c.-20G>A NP_001121100.1:n.-20G>A
XM_006717005.2:c.-77+714G>A XP_006717068.1:n.-77+714G>A
XM_006717005.4:c.-77+714G>A XP_006717068.1:n.-77+714G>A
NM_000507.4:c.-20G>A MANE Select NP_000498.2:n.-20G>A
NM_001127628.2:c.-20G>A NP_001121100.1:n.-20G>A