Canonical Allele Identifier: CA497362085

Gene: CYBA

Linked Data

• gnomAD v4: 16-88643392-G-A
• MyVariant Identifiers: chr16:g.88709800G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88643392G>A , CM000678.2:g.88643392G>A	GRCh38
NC_000016.9:g.88709800G>A , CM000678.1:g.88709800G>A	GRCh37
NC_000016.8:g.87237301G>A	NCBI36
NG_007291.1:g.12658C>T , LRG_52:g.12658C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696156.1:c.465C>T	ENSP00000512446.1:p.Pro155=
ENST00000696157.1:c.*766C>T	ENSP00000512447.1:n.*766C>T
ENST00000696158.1:c.*803C>T	ENSP00000512448.1:n.*803C>T
ENST00000696159.1:c.*472C>T	ENSP00000512449.1:n.*472C>T
ENST00000696160.1:c.576C>T	ENSP00000512450.1:p.Pro192=
ENST00000696161.1:c.679C>T	ENSP00000512451.1:p.Pro227Ser
ENST00000696162.1:c.*1268C>T	ENSP00000512452.1:n.*1268C>T
ENST00000696163.1:c.498C>T	ENSP00000512453.1:p.Pro166=
ENST00000261623.8:c.549C>T MANE Select	ENSP00000261623.3:p.Pro183=
ENST00000261623.7:c.549C>T	ENSP00000261623.3:p.Pro183=
NM_000101.3:c.549C>T	NP_000092.2:p.Pro183=
NM_000101.4:c.549C>T MANE Select	NP_000092.2:p.Pro183=