Canonical Allele Identifier: CA196553530

Gene: FBP1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000682520.1:c.831T>C	ENSP00000507547.1:n.831T>C
ENST00000375326.9:c.671T>C MANE Select	ENSP00000364475.5:p.Val224Ala
ENST00000648117.1:c.476T>C	ENSP00000498145.1:p.Val159Ala
ENST00000375326.8:c.671T>C	ENSP00000364475.4:p.Val224Ala
ENST00000414122.1:c.419T>C	ENSP00000411619.1:p.Val140Ala
ENST00000415431.5:c.671T>C	ENSP00000408025.1:p.Val224Ala
NM_000507.3:c.671T>C	NP_000498.2:p.Val224Ala
NM_001127628.1:c.671T>C	NP_001121100.1:p.Val224Ala
XM_006717005.2:c.425T>C	XP_006717068.1:p.Val142Ala
XM_006717005.4:c.425T>C	XP_006717068.1:p.Val142Ala
NM_000507.4:c.671T>C MANE Select	NP_000498.2:p.Val224Ala
NM_001127628.2:c.671T>C	NP_001121100.1:p.Val224Ala