Canonical Allele Identifier: CA466099869
Gene: FBP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.97367847A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94605565A>G , CM000671.2:g.94605565A>G GRCh38
NC_000009.11:g.97367847A>G , CM000671.1:g.97367847A>G GRCh37
NC_000009.10:g.96407668A>G NCBI36
NG_008174.1:g.39685T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000682520.1:c.877T>C ENSP00000507547.1:n.877T>C
ENST00000375326.9:c.717T>C MANE Select ENSP00000364475.5:p.Ala239=
ENST00000648117.1:c.522T>C ENSP00000498145.1:p.Ala174=
ENST00000375326.8:c.717T>C ENSP00000364475.4:p.Ala239=
ENST00000415431.5:c.717T>C ENSP00000408025.1:p.Ala239=
NM_000507.3:c.717T>C NP_000498.2:p.Ala239=
NM_001127628.1:c.717T>C NP_001121100.1:p.Ala239=
XM_006717005.2:c.471T>C XP_006717068.1:p.Ala157=
XM_006717005.4:c.471T>C XP_006717068.1:p.Ala157=
NM_000507.4:c.717T>C MANE Select NP_000498.2:p.Ala239=
NM_001127628.2:c.717T>C NP_001121100.1:p.Ala239=