Canonical Allele Identifier: CA725611897

Gene: CYBA

Linked Data

• dbSNP Id: rs1282008439
• gnomAD v4: 16-88643298-C-T
• MyVariant Identifiers: chr16:g.88709706C>T (hg19) ; chr16:g.88643298C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88643298C>T , CM000678.2:g.88643298C>T	GRCh38
NC_000016.9:g.88709706C>T , CM000678.1:g.88709706C>T	GRCh37
NC_000016.8:g.87237207C>T	NCBI36
NG_007291.1:g.12752G>A , LRG_52:g.12752G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696156.1:c.*55G>A	ENSP00000512446.1:n.*55G>A
ENST00000696157.1:c.*860G>A	ENSP00000512447.1:n.*860G>A
ENST00000696158.1:c.*897G>A	ENSP00000512448.1:n.*897G>A
ENST00000696159.1:c.*566G>A	ENSP00000512449.1:n.*566G>A
ENST00000696160.1:c.*55G>A	ENSP00000512450.1:n.*55G>A
ENST00000696161.1:c.*8G>A	ENSP00000512451.1:n.*8G>A
ENST00000696162.1:c.*1362G>A	ENSP00000512452.1:n.*1362G>A
ENST00000696163.1:c.*55G>A	ENSP00000512453.1:n.*55G>A
ENST00000261623.8:c.*55G>A MANE Select	ENSP00000261623.3:n.*55G>A
ENST00000261623.7:c.*55G>A	ENSP00000261623.3:n.*55G>A
NM_000101.3:c.*55G>A	NP_000092.2:n.*55G>A
NM_000101.4:c.*55G>A MANE Select	NP_000092.2:n.*55G>A