Canonical Allele Identifier: CA466100862
Gene: FBP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.97372281G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94609999G>T , CM000671.2:g.94609999G>T GRCh38
NC_000009.11:g.97372281G>T , CM000671.1:g.97372281G>T GRCh37
NC_000009.10:g.96412102G>T NCBI36
NG_008174.1:g.35251C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682520.1:c.489C>A ENSP00000507547.1:p.Ala163=
ENST00000375326.9:c.489C>A MANE Select ENSP00000364475.5:p.Ala163=
ENST00000648117.1:c.294C>A ENSP00000498145.1:p.Ala98=
ENST00000375326.8:c.489C>A ENSP00000364475.4:p.Ala163=
ENST00000414122.1:c.237C>A ENSP00000411619.1:p.Ala79=
ENST00000415431.5:c.489C>A ENSP00000408025.1:p.Ala163=
NM_000507.3:c.489C>A NP_000498.2:p.Ala163=
NM_001127628.1:c.489C>A NP_001121100.1:p.Ala163=
XM_006717005.2:c.243C>A XP_006717068.1:p.Ala81=
XM_006717005.4:c.243C>A XP_006717068.1:p.Ala81=
NM_000507.4:c.489C>A MANE Select NP_000498.2:p.Ala163=
NM_001127628.2:c.489C>A NP_001121100.1:p.Ala163=