Canonical Allele Identifier: CA374107610

Gene: FBP1

Linked Data

• MyVariant Identifiers: chr9:g.97372208C>G (hg19) ; chr9:g.94609926C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94609926C>G , CM000671.2:g.94609926C>G	GRCh38
NC_000009.11:g.97372208C>G , CM000671.1:g.97372208C>G	GRCh37
NC_000009.10:g.96412029C>G	NCBI36
NG_008174.1:g.35324G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682520.1:c.562G>C	ENSP00000507547.1:p.Asp188His
ENST00000375326.9:c.562G>C MANE Select	ENSP00000364475.5:p.Asp188His
ENST00000648117.1:c.367G>C	ENSP00000498145.1:p.Asp123His
ENST00000375326.8:c.562G>C	ENSP00000364475.4:p.Asp188His
ENST00000414122.1:c.310G>C	ENSP00000411619.1:p.Asp104His
ENST00000415431.5:c.562G>C	ENSP00000408025.1:p.Asp188His
NM_000507.3:c.562G>C	NP_000498.2:p.Asp188His
NM_001127628.1:c.562G>C	NP_001121100.1:p.Asp188His
XM_006717005.2:c.316G>C	XP_006717068.1:p.Asp106His
XM_006717005.4:c.316G>C	XP_006717068.1:p.Asp106His
NM_000507.4:c.562G>C MANE Select	NP_000498.2:p.Asp188His
NM_001127628.2:c.562G>C	NP_001121100.1:p.Asp188His