Canonical Allele Identifier: CA466102927
Gene: FBP1 HGNC NCBI

Linked Data

gnomAD v4: 9-94620410-G-A
MyVariant Identifiers: chr9:g.97382692G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94620410G>A , CM000671.2:g.94620410G>A GRCh38
NC_000009.11:g.97382692G>A , CM000671.1:g.97382692G>A GRCh37
NC_000009.10:g.96422513G>A NCBI36
NG_008174.1:g.24840C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000682520.1:c.252C>T ENSP00000507547.1:p.Asn84=
ENST00000375326.9:c.252C>T MANE Select ENSP00000364475.5:p.Asn84=
ENST00000648117.1:c.150C>T ENSP00000498145.1:p.Asn50=
ENST00000375326.8:c.252C>T ENSP00000364475.4:p.Asn84=
ENST00000414122.1:c.-1C>T ENSP00000411619.1:n.-1C>T
ENST00000415431.5:c.252C>T ENSP00000408025.1:p.Asn84=
NM_000507.3:c.252C>T NP_000498.2:p.Asn84=
NM_001127628.1:c.252C>T NP_001121100.1:p.Asn84=
XM_006717005.2:c.6C>T XP_006717068.1:p.Asn2=
XM_006717005.4:c.6C>T XP_006717068.1:p.Asn2=
NM_000507.4:c.252C>T MANE Select NP_000498.2:p.Asn84=
NM_001127628.2:c.252C>T NP_001121100.1:p.Asn84=