Canonical Allele Identifier: CA515669156

Gene: CYBB

Linked Data

• MyVariant Identifiers: chrX:g.37642754A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37783501A>C , CM000685.2:g.37783501A>C	GRCh38
NC_000023.10:g.37642754A>C , CM000685.1:g.37642754A>C	GRCh37
NC_000023.9:g.37527698A>C	NCBI36
NG_009065.1:g.8485A>C , LRG_53:g.8485A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.153A>C	ENSP00000512461.1:p.Ala51=
ENST00000696171.1:c.57A>C	ENSP00000512462.1:p.Ala19=
ENST00000696172.1:c.153A>C	ENSP00000512463.1:p.Ala51=
ENST00000696173.1:n.161A>C
ENST00000378588.5:c.153A>C MANE Select	ENSP00000367851.4:p.Ala51=
ENST00000378588.4:c.153A>C	ENSP00000367851.4:p.Ala51=
ENST00000465127.1:c.171+357501A>C	ENSP00000417050.1:n.171+357501A>C
NM_000397.3:c.153A>C , LRG_53t1:c.153A>C	NP_000388.2:p.Ala51=
XM_011543890.1:c.-278A>C	XP_011542192.1:n.-278A>C
NM_000397.4:c.153A>C MANE Select	NP_000388.2:p.Ala51=