Canonical Allele Identifier: CA374106519

Gene: FBP1

Linked Data

• ClinVar Variation Id: 2875401
• ClinVar RCV Id: RCV003600187
• dbSNP Id: rs764292673
• MyVariant Identifiers: chr9:g.97367841A>C (hg19) ; chr9:g.94605559A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94605559A>C , CM000671.2:g.94605559A>C	GRCh38
NC_000009.11:g.97367841A>C , CM000671.1:g.97367841A>C	GRCh37
NC_000009.10:g.96407662A>C	NCBI36
NG_008174.1:g.39691T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682520.1:c.883T>G	ENSP00000507547.1:n.883T>G
ENST00000375326.9:c.723T>G MANE Select	ENSP00000364475.5:p.Tyr241Ter
ENST00000648117.1:c.528T>G	ENSP00000498145.1:p.Tyr176Ter
ENST00000375326.8:c.723T>G	ENSP00000364475.4:p.Tyr241Ter
ENST00000415431.5:c.723T>G	ENSP00000408025.1:p.Tyr241Ter
NM_000507.3:c.723T>G	NP_000498.2:p.Tyr241Ter
NM_001127628.1:c.723T>G	NP_001121100.1:p.Tyr241Ter
XM_006717005.2:c.477T>G	XP_006717068.1:p.Tyr159Ter
XM_006717005.4:c.477T>G	XP_006717068.1:p.Tyr159Ter
NM_000507.4:c.723T>G MANE Select	NP_000498.2:p.Tyr241Ter
NM_001127628.2:c.723T>G	NP_001121100.1:p.Tyr241Ter