Canonical Allele Identifier: CA1865227979
Gene: FBP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94609919A= , CM000671.2:g.94609919A= GRCh38
NC_000009.11:g.97372201A= , CM000671.1:g.97372201A= GRCh37
NC_000009.10:g.96412022A= NCBI36
NG_008174.1:g.35331T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682520.1:c.567+2T= ENSP00000507547.1:n.567+2T=
ENST00000375326.9:c.567+2T= MANE Select ENSP00000364475.5:n.567+2T=
ENST00000648117.1:c.372+2T= ENSP00000498145.1:n.372+2T=
ENST00000375326.8:c.567+2T= ENSP00000364475.4:n.567+2T=
ENST00000414122.1:c.315+2T= ENSP00000411619.1:n.315+2T=
ENST00000415431.5:c.567+2T= ENSP00000408025.1:n.567+2T=
NM_000507.3:c.567+2T= NP_000498.2:n.567+2T=
NM_001127628.1:c.567+2T= NP_001121100.1:n.567+2T=
XM_006717005.2:c.321+2T= XP_006717068.1:n.321+2T=
XM_006717005.4:c.321+2T= XP_006717068.1:n.321+2T=
NM_000507.4:c.567+2T= MANE Select NP_000498.2:n.567+2T=
NM_001127628.2:c.567+2T= NP_001121100.1:n.567+2T=