Canonical Allele Identifier: CA2690771497
Gene: FBP1 HGNC NCBI

Linked Data

gnomAD v4: 9-94639407-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94639407G>T , CM000671.2:g.94639407G>T GRCh38
NC_000009.11:g.97401689G>T , CM000671.1:g.97401689G>T GRCh37
NC_000009.10:g.96441510G>T NCBI36
NG_008174.1:g.5843C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375326.9:c.-97C>A MANE Select ENSP00000364475.5:n.-97C>A
ENST00000375326.8:c.-97C>A ENSP00000364475.4:n.-97C>A
ENST00000414122.1:c.-83+637C>A ENSP00000411619.1:n.-83+637C>A
ENST00000415431.5:c.-24-73C>A ENSP00000408025.1:n.-24-73C>A
NM_000507.3:c.-97C>A NP_000498.2:n.-97C>A
NM_001127628.1:c.-24-73C>A NP_001121100.1:n.-24-73C>A
XM_006717005.2:c.-77+637C>A XP_006717068.1:n.-77+637C>A
XM_006717005.4:c.-77+637C>A XP_006717068.1:n.-77+637C>A
NM_000507.4:c.-97C>A MANE Select NP_000498.2:n.-97C>A
NM_001127628.2:c.-24-73C>A NP_001121100.1:n.-24-73C>A
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