Canonical Allele Identifier: CA5136041

Gene: FBP1

Linked Data

• dbSNP Id: rs752198321
• ExAC: 9:97365631 G / C
• gnomAD v2: 9-97365631-G-C
• gnomAD v4: 9-94603349-G-C
• MyVariant Identifiers: chr9:g.97365631G>C (hg19) ; chr9:g.94603349G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94603349G>C , CM000671.2:g.94603349G>C	GRCh38
NC_000009.11:g.97365631G>C , CM000671.1:g.97365631G>C	GRCh37
NC_000009.10:g.96405452G>C	NCBI36
NG_008174.1:g.41901C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682520.1:c.1209C>G	ENSP00000507547.1:n.1209C>G
ENST00000375326.9:c.*32C>G MANE Select	ENSP00000364475.5:n.*32C>G
ENST00000648117.1:c.*32C>G	ENSP00000498145.1:n.*32C>G
ENST00000375326.8:c.*32C>G	ENSP00000364475.4:n.*32C>G
ENST00000415431.5:c.*32C>G	ENSP00000408025.1:n.*32C>G
NM_000507.3:c.*32C>G	NP_000498.2:n.*32C>G
NM_001127628.1:c.*32C>G	NP_001121100.1:n.*32C>G
XM_006717005.2:c.*32C>G	XP_006717068.1:n.*32C>G
XM_006717005.4:c.*32C>G	XP_006717068.1:n.*32C>G
NM_000507.4:c.*32C>G MANE Select	NP_000498.2:n.*32C>G
NM_001127628.2:c.*32C>G	NP_001121100.1:n.*32C>G