Canonical Allele Identifier: CA1865227972
Gene: FBP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94609902C= , CM000671.2:g.94609902C= GRCh38
NC_000009.11:g.97372184C= , CM000671.1:g.97372184C= GRCh37
NC_000009.10:g.96412005C= NCBI36
NG_008174.1:g.35348G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682520.1:c.567+19G= ENSP00000507547.1:n.567+19G=
ENST00000375326.9:c.567+19G= MANE Select ENSP00000364475.5:n.567+19G=
ENST00000648117.1:c.372+19G= ENSP00000498145.1:n.372+19G=
ENST00000375326.8:c.567+19G= ENSP00000364475.4:n.567+19G=
ENST00000414122.1:c.315+19G= ENSP00000411619.1:n.315+19G=
ENST00000415431.5:c.567+19G= ENSP00000408025.1:n.567+19G=
NM_000507.3:c.567+19G= NP_000498.2:n.567+19G=
NM_001127628.1:c.567+19G= NP_001121100.1:n.567+19G=
XM_006717005.2:c.321+19G= XP_006717068.1:n.321+19G=
XM_006717005.4:c.321+19G= XP_006717068.1:n.321+19G=
NM_000507.4:c.567+19G= MANE Select NP_000498.2:n.567+19G=
NM_001127628.2:c.567+19G= NP_001121100.1:n.567+19G=