Canonical Allele Identifier: CA382628674
Gene: BCO2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112193677A>T , CM000673.2:g.112193677A>T GRCh38
NC_000011.9:g.112064400A>T , CM000673.1:g.112064400A>T GRCh37
NC_000011.8:g.111569610A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000357685.11:c.497A>T MANE Select ENSP00000350314.5:p.Glu166Val
ENST00000357685.9:c.497A>T ENSP00000350314.5:p.Glu166Val
ENST00000361053.8:c.497A>T ENSP00000354338.4:p.Glu166Val
ENST00000438022.5:c.395A>T ENSP00000414843.1:p.Glu132Val
ENST00000460924.6:n.589A>T
ENST00000494860.5:n.349A>T
ENST00000525987.5:n.840A>T
ENST00000526088.5:c.395A>T ENSP00000436615.1:p.Glu132Val
ENST00000527939.1:c.*139A>T ENSP00000436956.1:n.*139A>T
ENST00000530677.1:c.204A>T
ENST00000531169.5:c.395A>T ENSP00000437053.1:p.Glu132Val
ENST00000532593.5:c.182A>T ENSP00000431802.1:p.Glu61Val
ENST00000532612.5:c.427A>T
ENST00000534122.5:n.1112A>T
ENST00000534550.5:c.*139A>T ENSP00000434488.1:n.*139A>T
NM_001037290.2:c.395A>T NP_001032367.2:p.Glu132Val
NM_001256397.1:c.395A>T NP_001243326.1:p.Glu132Val
NM_001256398.1:c.497A>T NP_001243327.1:p.Glu166Val
NM_001256400.1:c.182A>T NP_001243329.1:p.Glu61Val
NM_031938.5:c.497A>T NP_114144.4:p.Glu166Val
NM_001037290.3:c.395A>T NP_001032367.3:p.Glu132Val
NM_001256397.2:c.395A>T NP_001243326.2:p.Glu132Val
NM_001256398.2:c.497A>T NP_001243327.2:p.Glu166Val
NM_001256400.2:c.182A>T NP_001243329.2:p.Glu61Val
NM_031938.7:c.497A>T MANE Select NP_114144.5:p.Glu166Val
NM_001037290.4:c.395A>T NP_001032367.3:p.Glu132Val
NM_001256397.3:c.395A>T NP_001243326.2:p.Glu132Val
NM_001256398.3:c.497A>T NP_001243327.2:p.Glu166Val
NM_001256400.3:c.182A>T NP_001243329.2:p.Glu61Val