Canonical Allele Identifier: CA515672738

Gene: CYBB

Linked Data

• MyVariant Identifiers: chrX:g.37658265T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37799012T>C , CM000685.2:g.37799012T>C	GRCh38
NC_000023.10:g.37658265T>C , CM000685.1:g.37658265T>C	GRCh37
NC_000023.9:g.37543205T>C	NCBI36
NG_009065.1:g.23992T>C , LRG_53:g.23992T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.*241T>C	ENSP00000512461.1:n.*241T>C
ENST00000696171.1:c.636T>C	ENSP00000512462.1:p.Cys212=
ENST00000696172.1:c.*8T>C	ENSP00000512463.1:n.*8T>C
ENST00000378588.5:c.732T>C MANE Select	ENSP00000367851.4:p.Cys244=
ENST00000378588.4:c.732T>C	ENSP00000367851.4:p.Cys244=
ENST00000465127.1:c.171+373012T>C	ENSP00000417050.1:n.171+373012T>C
ENST00000492288.1:n.157T>C
NM_000397.3:c.732T>C , LRG_53t1:c.732T>C	NP_000388.2:p.Cys244=
XM_011543890.1:c.426T>C	XP_011542192.1:p.Cys142=
NM_000397.4:c.732T>C MANE Select	NP_000388.2:p.Cys244=