Canonical Allele Identifier: CA515671142

Gene: CYBB

Linked Data

• MyVariant Identifiers: chrX:g.37655314G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37796061G>C , CM000685.2:g.37796061G>C	GRCh38
NC_000023.10:g.37655314G>C , CM000685.1:g.37655314G>C	GRCh37
NC_000023.9:g.37540254G>C	NCBI36
NG_009065.1:g.21041G>C , LRG_53:g.21041G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.*103G>C	ENSP00000512461.1:n.*103G>C
ENST00000696171.1:c.498G>C	ENSP00000512462.1:p.Arg166=
ENST00000696172.1:c.338-2894G>C	ENSP00000512463.1:n.338-2894G>C
ENST00000378588.5:c.594G>C MANE Select	ENSP00000367851.4:p.Arg198=
ENST00000378588.4:c.594G>C	ENSP00000367851.4:p.Arg198=
ENST00000465127.1:c.171+370061G>C	ENSP00000417050.1:n.171+370061G>C
NM_000397.3:c.594G>C , LRG_53t1:c.594G>C	NP_000388.2:p.Arg198=
XM_011543890.1:c.288G>C	XP_011542192.1:p.Arg96=
NM_000397.4:c.594G>C MANE Select	NP_000388.2:p.Arg198=