Canonical Allele Identifier: CA1865226066
Gene: FBP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94605560T= , CM000671.2:g.94605560T= GRCh38
NC_000009.11:g.97367842T= , CM000671.1:g.97367842T= GRCh37
NC_000009.10:g.96407663T= NCBI36
NG_008174.1:g.39690A=

Transcript Alleles

HGVS Amino-acid change
ENST00000682520.1:c.882A= ENSP00000507547.1:n.882A=
ENST00000375326.9:c.722A= MANE Select ENSP00000364475.5:p.Tyr241=
ENST00000648117.1:c.527A= ENSP00000498145.1:p.Tyr176=
ENST00000375326.8:c.722A= ENSP00000364475.4:p.Tyr241=
ENST00000415431.5:c.722A= ENSP00000408025.1:p.Tyr241=
NM_000507.3:c.722A= NP_000498.2:p.Tyr241=
NM_001127628.1:c.722A= NP_001121100.1:p.Tyr241=
XM_006717005.2:c.476A= XP_006717068.1:p.Tyr159=
XM_006717005.4:c.476A= XP_006717068.1:p.Tyr159=
NM_000507.4:c.722A= MANE Select NP_000498.2:p.Tyr241=
NM_001127628.2:c.722A= NP_001121100.1:p.Tyr241=