Canonical Allele Identifier: CA515669199

Gene: CYBB

Linked Data

• gnomAD v4: X-37783558-A-T
• MyVariant Identifiers: chrX:g.37642811A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37783558A>T , CM000685.2:g.37783558A>T	GRCh38
NC_000023.10:g.37642811A>T , CM000685.1:g.37642811A>T	GRCh37
NC_000023.9:g.37527755A>T	NCBI36
NG_009065.1:g.8542A>T , LRG_53:g.8542A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.210A>T	ENSP00000512461.1:p.Pro70=
ENST00000696171.1:c.114A>T	ENSP00000512462.1:p.Pro38=
ENST00000696172.1:c.210A>T	ENSP00000512463.1:p.Pro70=
ENST00000696173.1:n.218A>T
ENST00000378588.5:c.210A>T MANE Select	ENSP00000367851.4:p.Pro70=
ENST00000378588.4:c.210A>T	ENSP00000367851.4:p.Pro70=
ENST00000465127.1:c.171+357558A>T	ENSP00000417050.1:n.171+357558A>T
NM_000397.3:c.210A>T , LRG_53t1:c.210A>T	NP_000388.2:p.Pro70=
XM_011543890.1:c.-221A>T	XP_011542192.1:n.-221A>T
NM_000397.4:c.210A>T MANE Select	NP_000388.2:p.Pro70=