Canonical Allele Identifier: CA374106512

Gene: FBP1

Linked Data

• dbSNP Id: rs1388609291
• gnomAD v2: 9-97367837-C-A
• gnomAD v4: 9-94605555-C-A
• MyVariant Identifiers: chr9:g.97367837C>A (hg19) ; chr9:g.94605555C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94605555C>A , CM000671.2:g.94605555C>A	GRCh38
NC_000009.11:g.97367837C>A , CM000671.1:g.97367837C>A	GRCh37
NC_000009.10:g.96407658C>A	NCBI36
NG_008174.1:g.39695G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682520.1:c.887G>T	ENSP00000507547.1:n.887G>T
ENST00000375326.9:c.727G>T MANE Select	ENSP00000364475.5:p.Ala243Ser
ENST00000648117.1:c.532G>T	ENSP00000498145.1:p.Ala178Ser
ENST00000375326.8:c.727G>T	ENSP00000364475.4:p.Ala243Ser
ENST00000415431.5:c.727G>T	ENSP00000408025.1:p.Ala243Ser
NM_000507.3:c.727G>T	NP_000498.2:p.Ala243Ser
NM_001127628.1:c.727G>T	NP_001121100.1:p.Ala243Ser
XM_006717005.2:c.481G>T	XP_006717068.1:p.Ala161Ser
XM_006717005.4:c.481G>T	XP_006717068.1:p.Ala161Ser
NM_000507.4:c.727G>T MANE Select	NP_000498.2:p.Ala243Ser
NM_001127628.2:c.727G>T	NP_001121100.1:p.Ala243Ser