Canonical Allele Identifier: CA515669182

Gene: CYBB

Linked Data

• gnomAD v4: X-37783531-T-C
• MyVariant Identifiers: chrX:g.37642784T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37783531T>C , CM000685.2:g.37783531T>C	GRCh38
NC_000023.10:g.37642784T>C , CM000685.1:g.37642784T>C	GRCh37
NC_000023.9:g.37527728T>C	NCBI36
NG_009065.1:g.8515T>C , LRG_53:g.8515T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.183T>C	ENSP00000512461.1:p.Asn61=
ENST00000696171.1:c.87T>C	ENSP00000512462.1:p.Asn29=
ENST00000696172.1:c.183T>C	ENSP00000512463.1:p.Asn61=
ENST00000696173.1:n.191T>C
ENST00000378588.5:c.183T>C MANE Select	ENSP00000367851.4:p.Asn61=
ENST00000378588.4:c.183T>C	ENSP00000367851.4:p.Asn61=
ENST00000465127.1:c.171+357531T>C	ENSP00000417050.1:n.171+357531T>C
NM_000397.3:c.183T>C , LRG_53t1:c.183T>C	NP_000388.2:p.Asn61=
XM_011543890.1:c.-248T>C	XP_011542192.1:n.-248T>C
NM_000397.4:c.183T>C MANE Select	NP_000388.2:p.Asn61=