Canonical Allele Identifier: CA466099558

Gene: FBP1

Linked Data

• dbSNP Id: rs1319792140
• gnomAD v2: 9-97367739-C-T
• MyVariant Identifiers: chr9:g.97367739C>T (hg19) ; chr9:g.94605457C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94605457C>T , CM000671.2:g.94605457C>T	GRCh38
NC_000009.11:g.97367739C>T , CM000671.1:g.97367739C>T	GRCh37
NC_000009.10:g.96407560C>T	NCBI36
NG_008174.1:g.39793G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682520.1:c.985G>A	ENSP00000507547.1:n.985G>A
ENST00000375326.9:c.825G>A MANE Select	ENSP00000364475.5:p.Lys275=
ENST00000648117.1:c.630G>A	ENSP00000498145.1:p.Lys210=
ENST00000375326.8:c.825G>A	ENSP00000364475.4:p.Lys275=
ENST00000415431.5:c.825G>A	ENSP00000408025.1:p.Lys275=
NM_000507.3:c.825G>A	NP_000498.2:p.Lys275=
NM_001127628.1:c.825G>A	NP_001121100.1:p.Lys275=
XM_006717005.2:c.579G>A	XP_006717068.1:p.Lys193=
XM_006717005.4:c.579G>A	XP_006717068.1:p.Lys193=
NM_000507.4:c.825G>A MANE Select	NP_000498.2:p.Lys275=
NM_001127628.2:c.825G>A	NP_001121100.1:p.Lys275=