Canonical Allele Identifier: CA515672779

Gene: CYBB

Linked Data

• MyVariant Identifiers: chrX:g.37658277C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37799024C>A , CM000685.2:g.37799024C>A	GRCh38
NC_000023.10:g.37658277C>A , CM000685.1:g.37658277C>A	GRCh37
NC_000023.9:g.37543217C>A	NCBI36
NG_009065.1:g.24004C>A , LRG_53:g.24004C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000696170.1:c.*253C>A	ENSP00000512461.1:n.*253C>A
ENST00000696171.1:c.648C>A	ENSP00000512462.1:p.Ile216=
ENST00000696172.1:c.*20C>A	ENSP00000512463.1:n.*20C>A
ENST00000378588.5:c.744C>A MANE Select	ENSP00000367851.4:p.Ile248=
ENST00000378588.4:c.744C>A	ENSP00000367851.4:p.Ile248=
ENST00000465127.1:c.171+373024C>A	ENSP00000417050.1:n.171+373024C>A
ENST00000492288.1:n.169C>A
NM_000397.3:c.744C>A , LRG_53t1:c.744C>A	NP_000388.2:p.Ile248=
XM_011543890.1:c.438C>A	XP_011542192.1:p.Ile146=
NM_000397.4:c.744C>A MANE Select	NP_000388.2:p.Ile248=