Canonical Allele Identifier: CA515670953

Gene: CYBB

Linked Data

• MyVariant Identifiers: chrX:g.37655287T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37796034T>C , CM000685.2:g.37796034T>C	GRCh38
NC_000023.10:g.37655287T>C , CM000685.1:g.37655287T>C	GRCh37
NC_000023.9:g.37540227T>C	NCBI36
NG_009065.1:g.21014T>C , LRG_53:g.21014T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.*76T>C	ENSP00000512461.1:n.*76T>C
ENST00000696171.1:c.471T>C	ENSP00000512462.1:p.Ile157=
ENST00000696172.1:c.338-2921T>C	ENSP00000512463.1:n.338-2921T>C
ENST00000378588.5:c.567T>C MANE Select	ENSP00000367851.4:p.Ile189=
ENST00000378588.4:c.567T>C	ENSP00000367851.4:p.Ile189=
ENST00000465127.1:c.171+370034T>C	ENSP00000417050.1:n.171+370034T>C
NM_000397.3:c.567T>C , LRG_53t1:c.567T>C	NP_000388.2:p.Ile189=
XM_011543890.1:c.261T>C	XP_011542192.1:p.Ile87=
NM_000397.4:c.567T>C MANE Select	NP_000388.2:p.Ile189=