Canonical Allele Identifier: CA658821566

Gene: FBP1

Linked Data

• ClinVar Variation Id: 561987
• ClinVar RCV Id: RCV000681448
• dbSNP Id: rs1563984164
• MyVariant Identifiers: chr9:g.97382612_97382774del (hg19) ; chr9:g.94620329_94620491del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94620330_94620492del , CM000671.2:g.94620330_94620492del	GRCh38
NC_000009.11:g.97382612_97382774del , CM000671.1:g.97382612_97382774del	GRCh37
NC_000009.10:g.96422433_96422595del	NCBI36
NG_008174.1:g.24759_24921del

Transcript Alleles

HGVS	Amino-acid change
ENST00000682520.1:c.171_333del
ENST00000375326.9:c.171_333del
ENST00000648117.1:c.69_231del
ENST00000375326.8:c.171_333del
ENST00000414122.1:c.-82_81del
ENST00000415431.5:c.171_333del
NM_000507.3:c.171_333del
NM_001127628.1:c.171_333del
XM_006717005.2:c.-76_87del
XM_006717005.4:c.-76_87del
NM_000507.4:c.171_333del
NM_001127628.2:c.171_333del