Canonical Allele Identifier: CA2579387265
Gene: FBP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94609904C>G , CM000671.2:g.94609904C>G GRCh38
NC_000009.11:g.97372186C>G , CM000671.1:g.97372186C>G GRCh37
NC_000009.10:g.96412007C>G NCBI36
NG_008174.1:g.35346G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000682520.1:c.567+17G>C ENSP00000507547.1:n.567+17G>C
ENST00000375326.9:c.567+17G>C MANE Select ENSP00000364475.5:n.567+17G>C
ENST00000648117.1:c.372+17G>C ENSP00000498145.1:n.372+17G>C
ENST00000375326.8:c.567+17G>C ENSP00000364475.4:n.567+17G>C
ENST00000414122.1:c.315+17G>C ENSP00000411619.1:n.315+17G>C
ENST00000415431.5:c.567+17G>C ENSP00000408025.1:n.567+17G>C
NM_000507.3:c.567+17G>C NP_000498.2:n.567+17G>C
NM_001127628.1:c.567+17G>C NP_001121100.1:n.567+17G>C
XM_006717005.2:c.321+17G>C XP_006717068.1:n.321+17G>C
XM_006717005.4:c.321+17G>C XP_006717068.1:n.321+17G>C
NM_000507.4:c.567+17G>C MANE Select NP_000498.2:n.567+17G>C
NM_001127628.2:c.567+17G>C NP_001121100.1:n.567+17G>C