Canonical Allele Identifier: CA515669192

Gene: CYBB

Linked Data

• MyVariant Identifiers: chrX:g.37642802T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37783549T>C , CM000685.2:g.37783549T>C	GRCh38
NC_000023.10:g.37642802T>C , CM000685.1:g.37642802T>C	GRCh37
NC_000023.9:g.37527746T>C	NCBI36
NG_009065.1:g.8533T>C , LRG_53:g.8533T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.201T>C	ENSP00000512461.1:p.Ile67=
ENST00000696171.1:c.105T>C	ENSP00000512462.1:p.Ile35=
ENST00000696172.1:c.201T>C	ENSP00000512463.1:p.Ile67=
ENST00000696173.1:n.209T>C
ENST00000378588.5:c.201T>C MANE Select	ENSP00000367851.4:p.Ile67=
ENST00000378588.4:c.201T>C	ENSP00000367851.4:p.Ile67=
ENST00000465127.1:c.171+357549T>C	ENSP00000417050.1:n.171+357549T>C
NM_000397.3:c.201T>C , LRG_53t1:c.201T>C	NP_000388.2:p.Ile67=
XM_011543890.1:c.-230T>C	XP_011542192.1:n.-230T>C
NM_000397.4:c.201T>C MANE Select	NP_000388.2:p.Ile67=