Canonical Allele Identifier: CA2241199546
Gene: CYBA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88643335G= , CM000678.2:g.88643335G= GRCh38
NC_000016.9:g.88709743G= , CM000678.1:g.88709743G= GRCh37
NC_000016.8:g.87237244G= NCBI36
NG_007291.1:g.12715C= , LRG_52:g.12715C=

Transcript Alleles

HGVS Amino-acid change
ENST00000696156.1:c.*18C= ENSP00000512446.1:n.*18C=
ENST00000696157.1:c.*823C= ENSP00000512447.1:n.*823C=
ENST00000696158.1:c.*860C= ENSP00000512448.1:n.*860C=
ENST00000696159.1:c.*529C= ENSP00000512449.1:n.*529C=
ENST00000696160.1:c.*18C= ENSP00000512450.1:n.*18C=
ENST00000696161.1:c.736C= ENSP00000512451.1:p.Pro246=
ENST00000696162.1:c.*1325C= ENSP00000512452.1:n.*1325C=
ENST00000696163.1:c.*18C= ENSP00000512453.1:n.*18C=
ENST00000261623.8:c.*18C= MANE Select ENSP00000261623.3:n.*18C=
ENST00000261623.7:c.*18C= ENSP00000261623.3:n.*18C=
NM_000101.3:c.*18C= NP_000092.2:n.*18C=
NM_000101.4:c.*18C= MANE Select NP_000092.2:n.*18C=