Canonical Allele Identifier: CA382628249

Gene: BCO2

Linked Data

• dbSNP Id: rs1867462200
• gnomAD v3: 11-112193487-T-A
• gnomAD v4: 11-112193487-T-A
• MyVariant Identifiers: chr11:g.112064210T>A (hg19) ; chr11:g.112193487T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112193487T>A , CM000673.2:g.112193487T>A	GRCh38
NC_000011.9:g.112064210T>A , CM000673.1:g.112064210T>A	GRCh37
NC_000011.8:g.111569420T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357685.11:c.307T>A MANE Select	ENSP00000350314.5:p.Phe103Ile
ENST00000357685.9:c.307T>A	ENSP00000350314.5:p.Phe103Ile
ENST00000361053.8:c.307T>A	ENSP00000354338.4:p.Phe103Ile
ENST00000438022.5:c.205T>A	ENSP00000414843.1:p.Phe69Ile
ENST00000460924.6:n.399T>A
ENST00000494860.5:n.159T>A
ENST00000525468.1:n.296T>A
ENST00000525987.5:n.650T>A
ENST00000526088.5:c.205T>A	ENSP00000436615.1:p.Phe69Ile
ENST00000527939.1:c.102T>A	ENSP00000436956.1:p.Gly34=
ENST00000530677.1:c.14T>A
ENST00000531003.1:c.*97T>A	ENSP00000435869.1:n.*97T>A
ENST00000531169.5:c.205T>A	ENSP00000437053.1:p.Phe69Ile
ENST00000532593.5:c.-9T>A	ENSP00000431802.1:n.-9T>A
ENST00000532612.5:c.237T>A
ENST00000532699.1:c.*69T>A	ENSP00000456434.1:n.*69T>A
ENST00000534122.5:n.922T>A
ENST00000534550.5:c.102T>A	ENSP00000434488.1:p.Gly34=
NM_001037290.2:c.205T>A	NP_001032367.2:p.Phe69Ile
NM_001256397.1:c.205T>A	NP_001243326.1:p.Phe69Ile
NM_001256398.1:c.307T>A	NP_001243327.1:p.Phe103Ile
NM_001256400.1:c.-9T>A	NP_001243329.1:n.-9T>A
NM_031938.5:c.307T>A	NP_114144.4:p.Phe103Ile
NM_001037290.3:c.205T>A	NP_001032367.3:p.Phe69Ile
NM_001256397.2:c.205T>A	NP_001243326.2:p.Phe69Ile
NM_001256398.2:c.307T>A	NP_001243327.2:p.Phe103Ile
NM_001256400.2:c.-9T>A	NP_001243329.2:n.-9T>A
NM_031938.7:c.307T>A MANE Select	NP_114144.5:p.Phe103Ile
NM_001037290.4:c.205T>A	NP_001032367.3:p.Phe69Ile
NM_001256397.3:c.205T>A	NP_001243326.2:p.Phe69Ile
NM_001256398.3:c.307T>A	NP_001243327.2:p.Phe103Ile
NM_001256400.3:c.-9T>A	NP_001243329.2:n.-9T>A