Canonical Allele Identifier: CA382628298

Gene: BCO2

Linked Data

• MyVariant Identifiers: chr11:g.112064232A>G (hg19) ; chr11:g.112193509A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112193509A>G , CM000673.2:g.112193509A>G	GRCh38
NC_000011.9:g.112064232A>G , CM000673.1:g.112064232A>G	GRCh37
NC_000011.8:g.111569442A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357685.11:c.329A>G MANE Select	ENSP00000350314.5:p.His110Arg
ENST00000357685.9:c.329A>G	ENSP00000350314.5:p.His110Arg
ENST00000361053.8:c.329A>G	ENSP00000354338.4:p.His110Arg
ENST00000438022.5:c.227A>G	ENSP00000414843.1:p.His76Arg
ENST00000460924.6:n.421A>G
ENST00000494860.5:n.181A>G
ENST00000525468.1:n.318A>G
ENST00000525987.5:n.672A>G
ENST00000526088.5:c.227A>G	ENSP00000436615.1:p.His76Arg
ENST00000527939.1:c.124A>G	ENSP00000436956.1:p.Thr42Ala
ENST00000530677.1:c.36A>G
ENST00000531003.1:c.*119A>G	ENSP00000435869.1:n.*119A>G
ENST00000531169.5:c.227A>G	ENSP00000437053.1:p.His76Arg
ENST00000532593.5:c.14A>G	ENSP00000431802.1:p.His5Arg
ENST00000532612.5:c.259A>G
ENST00000532699.1:c.*91A>G	ENSP00000456434.1:n.*91A>G
ENST00000534122.5:n.944A>G
ENST00000534550.5:c.124A>G	ENSP00000434488.1:p.Thr42Ala
NM_001037290.2:c.227A>G	NP_001032367.2:p.His76Arg
NM_001256397.1:c.227A>G	NP_001243326.1:p.His76Arg
NM_001256398.1:c.329A>G	NP_001243327.1:p.His110Arg
NM_001256400.1:c.14A>G	NP_001243329.1:p.His5Arg
NM_031938.5:c.329A>G	NP_114144.4:p.His110Arg
NM_001037290.3:c.227A>G	NP_001032367.3:p.His76Arg
NM_001256397.2:c.227A>G	NP_001243326.2:p.His76Arg
NM_001256398.2:c.329A>G	NP_001243327.2:p.His110Arg
NM_001256400.2:c.14A>G	NP_001243329.2:p.His5Arg
NM_031938.7:c.329A>G MANE Select	NP_114144.5:p.His110Arg
NM_001037290.4:c.227A>G	NP_001032367.3:p.His76Arg
NM_001256397.3:c.227A>G	NP_001243326.2:p.His76Arg
NM_001256398.3:c.329A>G	NP_001243327.2:p.His110Arg
NM_001256400.3:c.14A>G	NP_001243329.2:p.His5Arg