Canonical Allele Identifier: CA374106697

Gene: FBP1

Linked Data

• dbSNP Id: rs967936941
• MyVariant Identifiers: chr9:g.97369131A>T (hg19) ; chr9:g.94606849A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94606849A>T , CM000671.2:g.94606849A>T	GRCh38
NC_000009.11:g.97369131A>T , CM000671.1:g.97369131A>T	GRCh37
NC_000009.10:g.96408952A>T	NCBI36
NG_008174.1:g.38401T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682520.1:c.831T>A	ENSP00000507547.1:n.831T>A
ENST00000375326.9:c.671T>A MANE Select	ENSP00000364475.5:p.Val224Asp
ENST00000648117.1:c.476T>A	ENSP00000498145.1:p.Val159Asp
ENST00000375326.8:c.671T>A	ENSP00000364475.4:p.Val224Asp
ENST00000414122.1:c.419T>A	ENSP00000411619.1:p.Val140Asp
ENST00000415431.5:c.671T>A	ENSP00000408025.1:p.Val224Asp
NM_000507.3:c.671T>A	NP_000498.2:p.Val224Asp
NM_001127628.1:c.671T>A	NP_001121100.1:p.Val224Asp
XM_006717005.2:c.425T>A	XP_006717068.1:p.Val142Asp
XM_006717005.4:c.425T>A	XP_006717068.1:p.Val142Asp
NM_000507.4:c.671T>A MANE Select	NP_000498.2:p.Val224Asp
NM_001127628.2:c.671T>A	NP_001121100.1:p.Val224Asp