Canonical Allele Identifier: CA2634847724

Gene: CYBA

Linked Data

• gnomAD v4: 16-88643333-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88643333A>G , CM000678.2:g.88643333A>G	GRCh38
NC_000016.9:g.88709741A>G , CM000678.1:g.88709741A>G	GRCh37
NC_000016.8:g.87237242A>G	NCBI36
NG_007291.1:g.12717T>C , LRG_52:g.12717T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000696156.1:c.*20T>C	ENSP00000512446.1:n.*20T>C
ENST00000696157.1:c.*825T>C	ENSP00000512447.1:n.*825T>C
ENST00000696158.1:c.*862T>C	ENSP00000512448.1:n.*862T>C
ENST00000696159.1:c.*531T>C	ENSP00000512449.1:n.*531T>C
ENST00000696160.1:c.*20T>C	ENSP00000512450.1:n.*20T>C
ENST00000696161.1:c.738T>C	ENSP00000512451.1:p.Pro246=
ENST00000696162.1:c.*1327T>C	ENSP00000512452.1:n.*1327T>C
ENST00000696163.1:c.*20T>C	ENSP00000512453.1:n.*20T>C
ENST00000261623.8:c.*20T>C MANE Select	ENSP00000261623.3:n.*20T>C
ENST00000261623.7:c.*20T>C	ENSP00000261623.3:n.*20T>C
NM_000101.3:c.*20T>C	NP_000092.2:n.*20T>C
NM_000101.4:c.*20T>C MANE Select	NP_000092.2:n.*20T>C