Canonical Allele Identifier: CA640895199

Gene: CYBB

Linked Data

• dbSNP Id: rs1556464908
• gnomAD v2: X-37642982-C-T
• MyVariant Identifiers: chrX:g.37642982C>T (hg19) ; chrX:g.37783729C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37783729C>T , CM000685.2:g.37783729C>T	GRCh38
NC_000023.10:g.37642982C>T , CM000685.1:g.37642982C>T	GRCh37
NC_000023.9:g.37527926C>T	NCBI36
NG_009065.1:g.8713C>T , LRG_53:g.8713C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.252+129C>T	ENSP00000512461.1:n.252+129C>T
ENST00000696171.1:c.156+129C>T	ENSP00000512462.1:n.156+129C>T
ENST00000696172.1:c.252+129C>T	ENSP00000512463.1:n.252+129C>T
ENST00000696173.1:n.260+129C>T
ENST00000378588.5:c.252+129C>T MANE Select	ENSP00000367851.4:n.252+129C>T
ENST00000378588.4:c.252+129C>T	ENSP00000367851.4:n.252+129C>T
ENST00000465127.1:c.171+357729C>T	ENSP00000417050.1:n.171+357729C>T
NM_000397.3:c.252+129C>T , LRG_53t1:c.252+129C>T	NP_000388.2:n.252+129C>T
XM_011543890.1:c.-179+129C>T	XP_011542192.1:n.-179+129C>T
NM_000397.4:c.252+129C>T MANE Select	NP_000388.2:n.252+129C>T