Canonical Allele Identifier: CA515670883

Gene: CYBB

Linked Data

• MyVariant Identifiers: chrX:g.37655272G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37796019G>C , CM000685.2:g.37796019G>C	GRCh38
NC_000023.10:g.37655272G>C , CM000685.1:g.37655272G>C	GRCh37
NC_000023.9:g.37540212G>C	NCBI36
NG_009065.1:g.20999G>C , LRG_53:g.20999G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.*61G>C	ENSP00000512461.1:n.*61G>C
ENST00000696171.1:c.456G>C	ENSP00000512462.1:p.Leu152=
ENST00000696172.1:c.338-2936G>C	ENSP00000512463.1:n.338-2936G>C
ENST00000378588.5:c.552G>C MANE Select	ENSP00000367851.4:p.Leu184=
ENST00000378588.4:c.552G>C	ENSP00000367851.4:p.Leu184=
ENST00000465127.1:c.171+370019G>C	ENSP00000417050.1:n.171+370019G>C
NM_000397.3:c.552G>C , LRG_53t1:c.552G>C	NP_000388.2:p.Leu184=
XM_011543890.1:c.246G>C	XP_011542192.1:p.Leu82=
NM_000397.4:c.552G>C MANE Select	NP_000388.2:p.Leu184=