Canonical Allele Identifier: CA466099851
Gene: FBP1 HGNC NCBI

Linked Data

dbSNP Id: rs1827685407
gnomAD v3: 9-94605556-C-T
gnomAD v4: 9-94605556-C-T
MyVariant Identifiers: chr9:g.97367838C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94605556C>T , CM000671.2:g.94605556C>T GRCh38
NC_000009.11:g.97367838C>T , CM000671.1:g.97367838C>T GRCh37
NC_000009.10:g.96407659C>T NCBI36
NG_008174.1:g.39694G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000682520.1:c.886G>A ENSP00000507547.1:n.886G>A
ENST00000375326.9:c.726G>A MANE Select ENSP00000364475.5:p.Gly242=
ENST00000648117.1:c.531G>A ENSP00000498145.1:p.Gly177=
ENST00000375326.8:c.726G>A ENSP00000364475.4:p.Gly242=
ENST00000415431.5:c.726G>A ENSP00000408025.1:p.Gly242=
NM_000507.3:c.726G>A NP_000498.2:p.Gly242=
NM_001127628.1:c.726G>A NP_001121100.1:p.Gly242=
XM_006717005.2:c.480G>A XP_006717068.1:p.Gly160=
XM_006717005.4:c.480G>A XP_006717068.1:p.Gly160=
NM_000507.4:c.726G>A MANE Select NP_000498.2:p.Gly242=
NM_001127628.2:c.726G>A NP_001121100.1:p.Gly242=