Canonical Allele Identifier: CA2241199531
Gene: CYBA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88643330G= , CM000678.2:g.88643330G= GRCh38
NC_000016.9:g.88709738G= , CM000678.1:g.88709738G= GRCh37
NC_000016.8:g.87237239G= NCBI36
NG_007291.1:g.12720C= , LRG_52:g.12720C=

Transcript Alleles

HGVS Amino-acid change
ENST00000696156.1:c.*23C= ENSP00000512446.1:n.*23C=
ENST00000696157.1:c.*828C= ENSP00000512447.1:n.*828C=
ENST00000696158.1:c.*865C= ENSP00000512448.1:n.*865C=
ENST00000696159.1:c.*534C= ENSP00000512449.1:n.*534C=
ENST00000696160.1:c.*23C= ENSP00000512450.1:n.*23C=
ENST00000696161.1:c.741C= ENSP00000512451.1:p.Pro247=
ENST00000696162.1:c.*1330C= ENSP00000512452.1:n.*1330C=
ENST00000696163.1:c.*23C= ENSP00000512453.1:n.*23C=
ENST00000261623.8:c.*23C= MANE Select ENSP00000261623.3:n.*23C=
ENST00000261623.7:c.*23C= ENSP00000261623.3:n.*23C=
NM_000101.3:c.*23C= NP_000092.2:n.*23C=
NM_000101.4:c.*23C= MANE Select NP_000092.2:n.*23C=