Canonical Allele Identifier: CA1865265632
Gene: FBP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94639470C= , CM000671.2:g.94639470C= GRCh38
NC_000009.11:g.97401752C= , CM000671.1:g.97401752C= GRCh37
NC_000009.10:g.96441573C= NCBI36
NG_008174.1:g.5780G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375326.9:c.-160G= MANE Select ENSP00000364475.5:n.-160G=
ENST00000375326.8:c.-160G= ENSP00000364475.4:n.-160G=
ENST00000414122.1:c.-83+574G= ENSP00000411619.1:n.-83+574G=
ENST00000415431.5:c.-24-136G= ENSP00000408025.1:n.-24-136G=
NM_000507.3:c.-160G= NP_000498.2:n.-160G=
NM_001127628.1:c.-24-136G= NP_001121100.1:n.-24-136G=
XM_006717005.2:c.-77+574G= XP_006717068.1:n.-77+574G=
XM_006717005.4:c.-77+574G= XP_006717068.1:n.-77+574G=
NM_000507.4:c.-160G= MANE Select NP_000498.2:n.-160G=
NM_001127628.2:c.-24-136G= NP_001121100.1:n.-24-136G=