Canonical Allele Identifier: CA2634847711

Gene: CYBA

Linked Data

• gnomAD v4: 16-88643326-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88643326T>G , CM000678.2:g.88643326T>G	GRCh38
NC_000016.9:g.88709734T>G , CM000678.1:g.88709734T>G	GRCh37
NC_000016.8:g.87237235T>G	NCBI36
NG_007291.1:g.12724A>C , LRG_52:g.12724A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696156.1:c.*27A>C	ENSP00000512446.1:n.*27A>C
ENST00000696157.1:c.*832A>C	ENSP00000512447.1:n.*832A>C
ENST00000696158.1:c.*869A>C	ENSP00000512448.1:n.*869A>C
ENST00000696159.1:c.*538A>C	ENSP00000512449.1:n.*538A>C
ENST00000696160.1:c.*27A>C	ENSP00000512450.1:n.*27A>C
ENST00000696161.1:c.745A>C	ENSP00000512451.1:p.Arg249=
ENST00000696162.1:c.*1334A>C	ENSP00000512452.1:n.*1334A>C
ENST00000696163.1:c.*27A>C	ENSP00000512453.1:n.*27A>C
ENST00000261623.8:c.*27A>C MANE Select	ENSP00000261623.3:n.*27A>C
ENST00000261623.7:c.*27A>C	ENSP00000261623.3:n.*27A>C
NM_000101.3:c.*27A>C	NP_000092.2:n.*27A>C
NM_000101.4:c.*27A>C MANE Select	NP_000092.2:n.*27A>C