Canonical Allele Identifier: CA412972712

Gene: CYBB

Linked Data

• gnomAD v4: X-37783499-G-A
• MyVariant Identifiers: chrX:g.37642752G>A (hg19) ; chrX:g.37783499G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37783499G>A , CM000685.2:g.37783499G>A	GRCh38
NC_000023.10:g.37642752G>A , CM000685.1:g.37642752G>A	GRCh37
NC_000023.9:g.37527696G>A	NCBI36
NG_009065.1:g.8483G>A , LRG_53:g.8483G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.151G>A	ENSP00000512461.1:p.Ala51Thr
ENST00000696171.1:c.55G>A	ENSP00000512462.1:p.Ala19Thr
ENST00000696172.1:c.151G>A	ENSP00000512463.1:p.Ala51Thr
ENST00000696173.1:n.159G>A
ENST00000378588.5:c.151G>A MANE Select	ENSP00000367851.4:p.Ala51Thr
ENST00000378588.4:c.151G>A	ENSP00000367851.4:p.Ala51Thr
ENST00000465127.1:c.171+357499G>A	ENSP00000417050.1:n.171+357499G>A
NM_000397.3:c.151G>A , LRG_53t1:c.151G>A	NP_000388.2:p.Ala51Thr
XM_011543890.1:c.-280G>A	XP_011542192.1:n.-280G>A
NM_000397.4:c.151G>A MANE Select	NP_000388.2:p.Ala51Thr