Canonical Allele Identifier: CA515677339

Gene: CYBB

Linked Data

• MyVariant Identifiers: chrX:g.37664277C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37805024C>G , CM000685.2:g.37805024C>G	GRCh38
NC_000023.10:g.37664277C>G , CM000685.1:g.37664277C>G	GRCh37
NC_000023.9:g.37549221C>G	NCBI36
NG_009065.1:g.30008C>G , LRG_53:g.30008C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000696170.1:c.*679C>G	ENSP00000512461.1:n.*679C>G
ENST00000696171.1:c.1074C>G	ENSP00000512462.1:p.Pro358=
ENST00000378588.5:c.1170C>G MANE Select	ENSP00000367851.4:p.Pro390=
ENST00000378588.4:c.1170C>G	ENSP00000367851.4:p.Pro390=
ENST00000465127.1:c.171+379024C>G	ENSP00000417050.1:n.171+379024C>G
NM_000397.3:c.1170C>G , LRG_53t1:c.1170C>G	NP_000388.2:p.Pro390=
XM_011543890.1:c.864C>G	XP_011542192.1:p.Pro288=
NM_000397.4:c.1170C>G MANE Select	NP_000388.2:p.Pro390=