Canonical Allele Identifier: CA515677252

Gene: CYBB

Linked Data

• MyVariant Identifiers: chrX:g.37664262A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37805009A>C , CM000685.2:g.37805009A>C	GRCh38
NC_000023.10:g.37664262A>C , CM000685.1:g.37664262A>C	GRCh37
NC_000023.9:g.37549206A>C	NCBI36
NG_009065.1:g.29993A>C , LRG_53:g.29993A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.*664A>C	ENSP00000512461.1:n.*664A>C
ENST00000696171.1:c.1059A>C	ENSP00000512462.1:p.Ile353=
ENST00000378588.5:c.1155A>C MANE Select	ENSP00000367851.4:p.Ile385=
ENST00000378588.4:c.1155A>C	ENSP00000367851.4:p.Ile385=
ENST00000465127.1:c.171+379009A>C	ENSP00000417050.1:n.171+379009A>C
NM_000397.3:c.1155A>C , LRG_53t1:c.1155A>C	NP_000388.2:p.Ile385=
XM_011543890.1:c.849A>C	XP_011542192.1:p.Ile283=
NM_000397.4:c.1155A>C MANE Select	NP_000388.2:p.Ile385=