Canonical Allele Identifier: CA286348055

Gene: CYBA

Linked Data

• dbSNP Id: rs1026088625
• gnomAD v2: 16-88709738-G-A
• gnomAD v3: 16-88643330-G-A
• gnomAD v4: 16-88643330-G-A
• MyVariant Identifiers: chr16:g.88709738G>A (hg19) ; chr16:g.88643330G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88643330G>A , CM000678.2:g.88643330G>A	GRCh38
NC_000016.9:g.88709738G>A , CM000678.1:g.88709738G>A	GRCh37
NC_000016.8:g.87237239G>A	NCBI36
NG_007291.1:g.12720C>T , LRG_52:g.12720C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000696156.1:c.*23C>T	ENSP00000512446.1:n.*23C>T
ENST00000696157.1:c.*828C>T	ENSP00000512447.1:n.*828C>T
ENST00000696158.1:c.*865C>T	ENSP00000512448.1:n.*865C>T
ENST00000696159.1:c.*534C>T	ENSP00000512449.1:n.*534C>T
ENST00000696160.1:c.*23C>T	ENSP00000512450.1:n.*23C>T
ENST00000696161.1:c.741C>T	ENSP00000512451.1:p.Pro247=
ENST00000696162.1:c.*1330C>T	ENSP00000512452.1:n.*1330C>T
ENST00000696163.1:c.*23C>T	ENSP00000512453.1:n.*23C>T
ENST00000261623.8:c.*23C>T MANE Select	ENSP00000261623.3:n.*23C>T
ENST00000261623.7:c.*23C>T	ENSP00000261623.3:n.*23C>T
NM_000101.3:c.*23C>T	NP_000092.2:n.*23C>T
NM_000101.4:c.*23C>T MANE Select	NP_000092.2:n.*23C>T