Canonical Allele Identifier: CA2241199526
Gene: CYBA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88643329C= , CM000678.2:g.88643329C= GRCh38
NC_000016.9:g.88709737C= , CM000678.1:g.88709737C= GRCh37
NC_000016.8:g.87237238C= NCBI36
NG_007291.1:g.12721G= , LRG_52:g.12721G=

Transcript Alleles

HGVS Amino-acid change
ENST00000696156.1:c.*24G= ENSP00000512446.1:n.*24G=
ENST00000696157.1:c.*829G= ENSP00000512447.1:n.*829G=
ENST00000696158.1:c.*866G= ENSP00000512448.1:n.*866G=
ENST00000696159.1:c.*535G= ENSP00000512449.1:n.*535G=
ENST00000696160.1:c.*24G= ENSP00000512450.1:n.*24G=
ENST00000696161.1:c.742G= ENSP00000512451.1:p.Ala248=
ENST00000696162.1:c.*1331G= ENSP00000512452.1:n.*1331G=
ENST00000696163.1:c.*24G= ENSP00000512453.1:n.*24G=
ENST00000261623.8:c.*24G= MANE Select ENSP00000261623.3:n.*24G=
ENST00000261623.7:c.*24G= ENSP00000261623.3:n.*24G=
NM_000101.3:c.*24G= NP_000092.2:n.*24G=
NM_000101.4:c.*24G= MANE Select NP_000092.2:n.*24G=