Canonical Allele Identifier: CA328041570

Gene: CYBB

Linked Data

• dbSNP Id: rs996176791
• MyVariant Identifiers: chrX:g.37803774G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37803774G>A , CM000685.2:g.37803774G>A	GRCh38
NC_000023.10:g.37663027G>A , CM000685.1:g.37663027G>A	GRCh37
NC_000023.9:g.37547971G>A	NCBI36
NG_009065.1:g.28758G>A , LRG_53:g.28758G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.*407-103G>A	ENSP00000512461.1:n.*407-103G>A
ENST00000696171.1:c.802-103G>A	ENSP00000512462.1:n.802-103G>A
ENST00000378588.5:c.898-103G>A MANE Select	ENSP00000367851.4:n.898-103G>A
ENST00000378588.4:c.898-103G>A	ENSP00000367851.4:n.898-103G>A
ENST00000465127.1:c.171+377774G>A	ENSP00000417050.1:n.171+377774G>A
ENST00000492288.1:n.323-103G>A
NM_000397.3:c.898-103G>A , LRG_53t1:c.898-103G>A	NP_000388.2:n.898-103G>A
XM_011543890.1:c.592-103G>A	XP_011542192.1:n.592-103G>A
NM_000397.4:c.898-103G>A MANE Select	NP_000388.2:n.898-103G>A