Canonical Allele Identifier: CA2241199533
Gene: CYBA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88643331G= , CM000678.2:g.88643331G= GRCh38
NC_000016.9:g.88709739G= , CM000678.1:g.88709739G= GRCh37
NC_000016.8:g.87237240G= NCBI36
NG_007291.1:g.12719C= , LRG_52:g.12719C=

Transcript Alleles

HGVS Amino-acid change
ENST00000696156.1:c.*22C= ENSP00000512446.1:n.*22C=
ENST00000696157.1:c.*827C= ENSP00000512447.1:n.*827C=
ENST00000696158.1:c.*864C= ENSP00000512448.1:n.*864C=
ENST00000696159.1:c.*533C= ENSP00000512449.1:n.*533C=
ENST00000696160.1:c.*22C= ENSP00000512450.1:n.*22C=
ENST00000696161.1:c.740C= ENSP00000512451.1:p.Pro247=
ENST00000696162.1:c.*1329C= ENSP00000512452.1:n.*1329C=
ENST00000696163.1:c.*22C= ENSP00000512453.1:n.*22C=
ENST00000261623.8:c.*22C= MANE Select ENSP00000261623.3:n.*22C=
ENST00000261623.7:c.*22C= ENSP00000261623.3:n.*22C=
NM_000101.3:c.*22C= NP_000092.2:n.*22C=
NM_000101.4:c.*22C= MANE Select NP_000092.2:n.*22C=