Canonical Allele Identifier: CA328040556

Gene: CYBB

Linked Data

• dbSNP Id: rs782502622
• gnomAD v3: X-37783910-G-A
• gnomAD v4: X-37783910-G-A
• MyVariant Identifiers: chrX:g.37643163G>A (hg19) ; chrX:g.37783910G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37783910G>A , CM000685.2:g.37783910G>A	GRCh38
NC_000023.10:g.37643163G>A , CM000685.1:g.37643163G>A	GRCh37
NC_000023.9:g.37528107G>A	NCBI36
NG_009065.1:g.8894G>A , LRG_53:g.8894G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.252+310G>A	ENSP00000512461.1:n.252+310G>A
ENST00000696171.1:c.156+310G>A	ENSP00000512462.1:n.156+310G>A
ENST00000696172.1:c.252+310G>A	ENSP00000512463.1:n.252+310G>A
ENST00000696173.1:n.260+310G>A
ENST00000378588.5:c.252+310G>A MANE Select	ENSP00000367851.4:n.252+310G>A
ENST00000378588.4:c.252+310G>A	ENSP00000367851.4:n.252+310G>A
ENST00000465127.1:c.171+357910G>A	ENSP00000417050.1:n.171+357910G>A
NM_000397.3:c.252+310G>A , LRG_53t1:c.252+310G>A	NP_000388.2:n.252+310G>A
XM_011543890.1:c.-179+310G>A	XP_011542192.1:n.-179+310G>A
NM_000397.4:c.252+310G>A MANE Select	NP_000388.2:n.252+310G>A