Canonical Allele Identifier: CA624182568

Gene: CYBA

Linked Data

• dbSNP Id: rs1001791471
• gnomAD v2: 16-88709710-G-T
• gnomAD v4: 16-88643302-G-T
• MyVariant Identifiers: chr16:g.88709710G>T (hg19) ; chr16:g.88643302G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88643302G>T , CM000678.2:g.88643302G>T	GRCh38
NC_000016.9:g.88709710G>T , CM000678.1:g.88709710G>T	GRCh37
NC_000016.8:g.87237211G>T	NCBI36
NG_007291.1:g.12748C>A , LRG_52:g.12748C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696156.1:c.*51C>A	ENSP00000512446.1:n.*51C>A
ENST00000696157.1:c.*856C>A	ENSP00000512447.1:n.*856C>A
ENST00000696158.1:c.*893C>A	ENSP00000512448.1:n.*893C>A
ENST00000696159.1:c.*562C>A	ENSP00000512449.1:n.*562C>A
ENST00000696160.1:c.*51C>A	ENSP00000512450.1:n.*51C>A
ENST00000696161.1:c.*4C>A	ENSP00000512451.1:n.*4C>A
ENST00000696162.1:c.*1358C>A	ENSP00000512452.1:n.*1358C>A
ENST00000696163.1:c.*51C>A	ENSP00000512453.1:n.*51C>A
ENST00000261623.8:c.*51C>A MANE Select	ENSP00000261623.3:n.*51C>A
ENST00000261623.7:c.*51C>A	ENSP00000261623.3:n.*51C>A
NM_000101.3:c.*51C>A	NP_000092.2:n.*51C>A
NM_000101.4:c.*51C>A MANE Select	NP_000092.2:n.*51C>A