Canonical Allele Identifier: CA466099966

Gene: FBP1

Linked Data

• MyVariant Identifiers: chr9:g.97369130G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94606848G>C , CM000671.2:g.94606848G>C	GRCh38
NC_000009.11:g.97369130G>C , CM000671.1:g.97369130G>C	GRCh37
NC_000009.10:g.96408951G>C	NCBI36
NG_008174.1:g.38402C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682520.1:c.832C>G	ENSP00000507547.1:n.832C>G
ENST00000375326.9:c.672C>G MANE Select	ENSP00000364475.5:p.Val224=
ENST00000648117.1:c.477C>G	ENSP00000498145.1:p.Val159=
ENST00000375326.8:c.672C>G	ENSP00000364475.4:p.Val224=
ENST00000414122.1:c.420C>G	ENSP00000411619.1:p.Val140=
ENST00000415431.5:c.672C>G	ENSP00000408025.1:p.Val224=
NM_000507.3:c.672C>G	NP_000498.2:p.Val224=
NM_001127628.1:c.672C>G	NP_001121100.1:p.Val224=
XM_006717005.2:c.426C>G	XP_006717068.1:p.Val142=
XM_006717005.4:c.426C>G	XP_006717068.1:p.Val142=
NM_000507.4:c.672C>G MANE Select	NP_000498.2:p.Val224=
NM_001127628.2:c.672C>G	NP_001121100.1:p.Val224=