Canonical Allele Identifier: CA875141435

Gene: CYBB

Linked Data

• dbSNP Id: rs1463626319
• gnomAD v3: X-37783919-A-T
• gnomAD v4: X-37783919-A-T
• MyVariant Identifiers: chrX:g.37783919A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37783919A>T , CM000685.2:g.37783919A>T	GRCh38
NC_000023.10:g.37643172A>T , CM000685.1:g.37643172A>T	GRCh37
NC_000023.9:g.37528116A>T	NCBI36
NG_009065.1:g.8903A>T , LRG_53:g.8903A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.252+319A>T	ENSP00000512461.1:n.252+319A>T
ENST00000696171.1:c.156+319A>T	ENSP00000512462.1:n.156+319A>T
ENST00000696172.1:c.252+319A>T	ENSP00000512463.1:n.252+319A>T
ENST00000696173.1:n.260+319A>T
ENST00000378588.5:c.252+319A>T MANE Select	ENSP00000367851.4:n.252+319A>T
ENST00000378588.4:c.252+319A>T	ENSP00000367851.4:n.252+319A>T
ENST00000465127.1:c.171+357919A>T	ENSP00000417050.1:n.171+357919A>T
NM_000397.3:c.252+319A>T , LRG_53t1:c.252+319A>T	NP_000388.2:n.252+319A>T
XM_011543890.1:c.-179+319A>T	XP_011542192.1:n.-179+319A>T
NM_000397.4:c.252+319A>T MANE Select	NP_000388.2:n.252+319A>T