Canonical Allele Identifier: CA196572437
Gene: FBP1 HGNC NCBI

Linked Data

dbSNP Id: rs1048185959
gnomAD v3: 9-94639437-C-T
gnomAD v4: 9-94639437-C-T
MyVariant Identifiers: chr9:g.94639437C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94639437C>T , CM000671.2:g.94639437C>T GRCh38
NC_000009.11:g.97401719C>T , CM000671.1:g.97401719C>T GRCh37
NC_000009.10:g.96441540C>T NCBI36
NG_008174.1:g.5813G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375326.9:c.-127G>A MANE Select ENSP00000364475.5:n.-127G>A
ENST00000375326.8:c.-127G>A ENSP00000364475.4:n.-127G>A
ENST00000414122.1:c.-83+607G>A ENSP00000411619.1:n.-83+607G>A
ENST00000415431.5:c.-24-103G>A ENSP00000408025.1:n.-24-103G>A
NM_000507.3:c.-127G>A NP_000498.2:n.-127G>A
NM_001127628.1:c.-24-103G>A NP_001121100.1:n.-24-103G>A
XM_006717005.2:c.-77+607G>A XP_006717068.1:n.-77+607G>A
XM_006717005.4:c.-77+607G>A XP_006717068.1:n.-77+607G>A
NM_000507.4:c.-127G>A MANE Select NP_000498.2:n.-127G>A
NM_001127628.2:c.-24-103G>A NP_001121100.1:n.-24-103G>A