Canonical Allele Identifier: CA374335122

Gene: FBP1

Linked Data

• dbSNP Id: rs1261230801
• gnomAD v2: 9-97401487-T-C
• gnomAD v3: 9-94639205-T-C
• gnomAD v4: 9-94639205-T-C
• MyVariant Identifiers: chr9:g.97401487T>C (hg19) ; chr9:g.94639205T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94639205T>C , CM000671.2:g.94639205T>C	GRCh38
NC_000009.11:g.97401487T>C , CM000671.1:g.97401487T>C	GRCh37
NC_000009.10:g.96441308T>C	NCBI36
NG_008174.1:g.6045A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682520.1:c.106A>G	ENSP00000507547.1:p.Asn36Asp
ENST00000375326.9:c.106A>G MANE Select	ENSP00000364475.5:p.Asn36Asp
ENST00000375326.8:c.106A>G	ENSP00000364475.4:p.Asn36Asp
ENST00000414122.1:c.-83+839A>G	ENSP00000411619.1:n.-83+839A>G
ENST00000415431.5:c.106A>G	ENSP00000408025.1:p.Asn36Asp
NM_000507.3:c.106A>G	NP_000498.2:p.Asn36Asp
NM_001127628.1:c.106A>G	NP_001121100.1:p.Asn36Asp
XM_006717005.2:c.-77+839A>G	XP_006717068.1:n.-77+839A>G
XM_006717005.4:c.-77+839A>G	XP_006717068.1:n.-77+839A>G
NM_000507.4:c.106A>G MANE Select	NP_000498.2:p.Asn36Asp
NM_001127628.2:c.106A>G	NP_001121100.1:p.Asn36Asp