Canonical Allele Identifier: CA466265740
Gene: FBP1 HGNC NCBI

Linked Data

gnomAD v4: 9-94639164-C-A
MyVariant Identifiers: chr9:g.97401446C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94639164C>A , CM000671.2:g.94639164C>A GRCh38
NC_000009.11:g.97401446C>A , CM000671.1:g.97401446C>A GRCh37
NC_000009.10:g.96441267C>A NCBI36
NG_008174.1:g.6086G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000682520.1:c.147G>T ENSP00000507547.1:p.Val49=
ENST00000375326.9:c.147G>T MANE Select ENSP00000364475.5:p.Val49=
ENST00000375326.8:c.147G>T ENSP00000364475.4:p.Val49=
ENST00000414122.1:c.-83+880G>T ENSP00000411619.1:n.-83+880G>T
ENST00000415431.5:c.147G>T ENSP00000408025.1:p.Val49=
NM_000507.3:c.147G>T NP_000498.2:p.Val49=
NM_001127628.1:c.147G>T NP_001121100.1:p.Val49=
XM_006717005.2:c.-77+880G>T XP_006717068.1:n.-77+880G>T
XM_006717005.4:c.-77+880G>T XP_006717068.1:n.-77+880G>T
NM_000507.4:c.147G>T MANE Select NP_000498.2:p.Val49=
NM_001127628.2:c.147G>T NP_001121100.1:p.Val49=