Canonical Allele Identifier: CA466099865
Gene: FBP1 HGNC NCBI

Linked Data

dbSNP Id: rs1827685646
gnomAD v3: 9-94605562-A-G
gnomAD v4: 9-94605562-A-G
MyVariant Identifiers: chr9:g.97367844A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94605562A>G , CM000671.2:g.94605562A>G GRCh38
NC_000009.11:g.97367844A>G , CM000671.1:g.97367844A>G GRCh37
NC_000009.10:g.96407665A>G NCBI36
NG_008174.1:g.39688T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000682520.1:c.880T>C ENSP00000507547.1:n.880T>C
ENST00000375326.9:c.720T>C MANE Select ENSP00000364475.5:p.Pro240=
ENST00000648117.1:c.525T>C ENSP00000498145.1:p.Pro175=
ENST00000375326.8:c.720T>C ENSP00000364475.4:p.Pro240=
ENST00000415431.5:c.720T>C ENSP00000408025.1:p.Pro240=
NM_000507.3:c.720T>C NP_000498.2:p.Pro240=
NM_001127628.1:c.720T>C NP_001121100.1:p.Pro240=
XM_006717005.2:c.474T>C XP_006717068.1:p.Pro158=
XM_006717005.4:c.474T>C XP_006717068.1:p.Pro158=
NM_000507.4:c.720T>C MANE Select NP_000498.2:p.Pro240=
NM_001127628.2:c.720T>C NP_001121100.1:p.Pro240=