Canonical Allele Identifier: CA374107599

Gene: FBP1

Linked Data

• dbSNP Id: rs1827757207
• MyVariant Identifiers: chr9:g.97372204G>T (hg19) ; chr9:g.94609922G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94609922G>T , CM000671.2:g.94609922G>T	GRCh38
NC_000009.11:g.97372204G>T , CM000671.1:g.97372204G>T	GRCh37
NC_000009.10:g.96412025G>T	NCBI36
NG_008174.1:g.35328C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682520.1:c.566C>A	ENSP00000507547.1:p.Pro189Gln
ENST00000375326.9:c.566C>A MANE Select	ENSP00000364475.5:p.Pro189Gln
ENST00000648117.1:c.371C>A	ENSP00000498145.1:p.Pro124Gln
ENST00000375326.8:c.566C>A	ENSP00000364475.4:p.Pro189Gln
ENST00000414122.1:c.314C>A	ENSP00000411619.1:p.Pro105Gln
ENST00000415431.5:c.566C>A	ENSP00000408025.1:p.Pro189Gln
NM_000507.3:c.566C>A	NP_000498.2:p.Pro189Gln
NM_001127628.1:c.566C>A	NP_001121100.1:p.Pro189Gln
XM_006717005.2:c.320C>A	XP_006717068.1:p.Pro107Gln
XM_006717005.4:c.320C>A	XP_006717068.1:p.Pro107Gln
NM_000507.4:c.566C>A MANE Select	NP_000498.2:p.Pro189Gln
NM_001127628.2:c.566C>A	NP_001121100.1:p.Pro189Gln