Canonical Allele Identifier: CA5136368

Gene: FBP1

Linked Data

• dbSNP Id: rs199970657
• ExAC: 9:97401602 G / T
• gnomAD v2: 9-97401602-G-T
• gnomAD v3: 9-94639320-G-T
• gnomAD v4: 9-94639320-G-T
• MyVariant Identifiers: chr9:g.97401602G>T (hg19) ; chr9:g.94639320G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94639320G>T , CM000671.2:g.94639320G>T	GRCh38
NC_000009.11:g.97401602G>T , CM000671.1:g.97401602G>T	GRCh37
NC_000009.10:g.96441423G>T	NCBI36
NG_008174.1:g.5930C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375326.9:c.-10C>A MANE Select	ENSP00000364475.5:n.-10C>A
ENST00000375326.8:c.-10C>A	ENSP00000364475.4:n.-10C>A
ENST00000414122.1:c.-83+724C>A	ENSP00000411619.1:n.-83+724C>A
ENST00000415431.5:c.-10C>A	ENSP00000408025.1:n.-10C>A
NM_000507.3:c.-10C>A	NP_000498.2:n.-10C>A
NM_001127628.1:c.-10C>A	NP_001121100.1:n.-10C>A
XM_006717005.2:c.-77+724C>A	XP_006717068.1:n.-77+724C>A
XM_006717005.4:c.-77+724C>A	XP_006717068.1:n.-77+724C>A
NM_000507.4:c.-10C>A MANE Select	NP_000498.2:n.-10C>A
NM_001127628.2:c.-10C>A	NP_001121100.1:n.-10C>A