Canonical Allele Identifier: CA640895204

Gene: CYBB

Linked Data

• dbSNP Id: rs1022677299
• gnomAD v2: X-37643124-C-A
• MyVariant Identifiers: chrX:g.37643124C>A (hg19) ; chrX:g.37783871C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37783871C>A , CM000685.2:g.37783871C>A	GRCh38
NC_000023.10:g.37643124C>A , CM000685.1:g.37643124C>A	GRCh37
NC_000023.9:g.37528068C>A	NCBI36
NG_009065.1:g.8855C>A , LRG_53:g.8855C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.252+271C>A	ENSP00000512461.1:n.252+271C>A
ENST00000696171.1:c.156+271C>A	ENSP00000512462.1:n.156+271C>A
ENST00000696172.1:c.252+271C>A	ENSP00000512463.1:n.252+271C>A
ENST00000696173.1:n.260+271C>A
ENST00000378588.5:c.252+271C>A MANE Select	ENSP00000367851.4:n.252+271C>A
ENST00000378588.4:c.252+271C>A	ENSP00000367851.4:n.252+271C>A
ENST00000465127.1:c.171+357871C>A	ENSP00000417050.1:n.171+357871C>A
NM_000397.3:c.252+271C>A , LRG_53t1:c.252+271C>A	NP_000388.2:n.252+271C>A
XM_011543890.1:c.-179+271C>A	XP_011542192.1:n.-179+271C>A
NM_000397.4:c.252+271C>A MANE Select	NP_000388.2:n.252+271C>A