Canonical Allele Identifier: CA497362089

Gene: CYBA

Linked Data

• dbSNP Id: rs1907151158
• gnomAD v3: 16-88643395-A-G
• gnomAD v4: 16-88643395-A-G
• MyVariant Identifiers: chr16:g.88709803A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88643395A>G , CM000678.2:g.88643395A>G	GRCh38
NC_000016.9:g.88709803A>G , CM000678.1:g.88709803A>G	GRCh37
NC_000016.8:g.87237304A>G	NCBI36
NG_007291.1:g.12655T>C , LRG_52:g.12655T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696156.1:c.462T>C	ENSP00000512446.1:p.Gly154=
ENST00000696157.1:c.*763T>C	ENSP00000512447.1:n.*763T>C
ENST00000696158.1:c.*800T>C	ENSP00000512448.1:n.*800T>C
ENST00000696159.1:c.*469T>C	ENSP00000512449.1:n.*469T>C
ENST00000696160.1:c.573T>C	ENSP00000512450.1:p.Gly191=
ENST00000696161.1:c.676T>C	ENSP00000512451.1:p.Ser226Pro
ENST00000696162.1:c.*1265T>C	ENSP00000512452.1:n.*1265T>C
ENST00000696163.1:c.495T>C	ENSP00000512453.1:p.Gly165=
ENST00000261623.8:c.546T>C MANE Select	ENSP00000261623.3:p.Gly182=
ENST00000261623.7:c.546T>C	ENSP00000261623.3:p.Gly182=
NM_000101.3:c.546T>C	NP_000092.2:p.Gly182=
NM_000101.4:c.546T>C MANE Select	NP_000092.2:p.Gly182=