Canonical Allele Identifier: CA624182581

Gene: CYBA

Linked Data

• dbSNP Id: rs1226872151
• gnomAD v2: 16-88709716-A-T
• gnomAD v4: 16-88643308-A-T
• MyVariant Identifiers: chr16:g.88709716A>T (hg19) ; chr16:g.88643308A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88643308A>T , CM000678.2:g.88643308A>T	GRCh38
NC_000016.9:g.88709716A>T , CM000678.1:g.88709716A>T	GRCh37
NC_000016.8:g.87237217A>T	NCBI36
NG_007291.1:g.12742T>A , LRG_52:g.12742T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696156.1:c.*45T>A	ENSP00000512446.1:n.*45T>A
ENST00000696157.1:c.*850T>A	ENSP00000512447.1:n.*850T>A
ENST00000696158.1:c.*887T>A	ENSP00000512448.1:n.*887T>A
ENST00000696159.1:c.*556T>A	ENSP00000512449.1:n.*556T>A
ENST00000696160.1:c.*45T>A	ENSP00000512450.1:n.*45T>A
ENST00000696161.1:c.763T>A	ENSP00000512451.1:p.Ter255Lys
ENST00000696162.1:c.*1352T>A	ENSP00000512452.1:n.*1352T>A
ENST00000696163.1:c.*45T>A	ENSP00000512453.1:n.*45T>A
ENST00000261623.8:c.*45T>A MANE Select	ENSP00000261623.3:n.*45T>A
ENST00000261623.7:c.*45T>A	ENSP00000261623.3:n.*45T>A
NM_000101.3:c.*45T>A	NP_000092.2:n.*45T>A
NM_000101.4:c.*45T>A MANE Select	NP_000092.2:n.*45T>A