Canonical Allele Identifier: CA397056792

Gene: CYBA

Linked Data

• MyVariant Identifiers: chr16:g.88709843T>C (hg19) ; chr16:g.88643435T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88643435T>C , CM000678.2:g.88643435T>C	GRCh38
NC_000016.9:g.88709843T>C , CM000678.1:g.88709843T>C	GRCh37
NC_000016.8:g.87237344T>C	NCBI36
NG_007291.1:g.12615A>G , LRG_52:g.12615A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696156.1:c.422A>G	ENSP00000512446.1:p.Glu141Gly
ENST00000696157.1:c.*723A>G	ENSP00000512447.1:n.*723A>G
ENST00000696158.1:c.*760A>G	ENSP00000512448.1:n.*760A>G
ENST00000696159.1:c.*429A>G	ENSP00000512449.1:n.*429A>G
ENST00000696160.1:c.533A>G	ENSP00000512450.1:p.Glu178Gly
ENST00000696161.1:c.636A>G	ENSP00000512451.1:p.Arg212=
ENST00000696162.1:c.*1225A>G	ENSP00000512452.1:n.*1225A>G
ENST00000696163.1:c.455A>G	ENSP00000512453.1:p.Glu152Gly
ENST00000261623.8:c.506A>G MANE Select	ENSP00000261623.3:p.Glu169Gly
ENST00000261623.7:c.506A>G	ENSP00000261623.3:p.Glu169Gly
NM_000101.3:c.506A>G	NP_000092.2:p.Glu169Gly
NM_000101.4:c.506A>G MANE Select	NP_000092.2:p.Glu169Gly