Canonical Allele Identifier: CA328041151
Gene: CYBB HGNC NCBI

Linked Data

dbSNP Id: rs983935810
gnomAD v4: X-37796204-A-G
MyVariant Identifiers: chrX:g.37796204A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37796204A>G , CM000685.2:g.37796204A>G GRCh38
NC_000023.10:g.37655457A>G , CM000685.1:g.37655457A>G GRCh37
NC_000023.9:g.37540397A>G NCBI36
NG_009065.1:g.21184A>G , LRG_53:g.21184A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696170.1:c.*183+63A>G ENSP00000512461.1:n.*183+63A>G
ENST00000696171.1:c.578+63A>G ENSP00000512462.1:n.578+63A>G
ENST00000696172.1:c.338-2751A>G ENSP00000512463.1:n.338-2751A>G
ENST00000378588.5:c.674+63A>G MANE Select ENSP00000367851.4:n.674+63A>G
ENST00000378588.4:c.674+63A>G ENSP00000367851.4:n.674+63A>G
ENST00000465127.1:c.171+370204A>G ENSP00000417050.1:n.171+370204A>G
NM_000397.3:c.674+63A>G , LRG_53t1:c.674+63A>G NP_000388.2:n.674+63A>G
XM_011543890.1:c.368+63A>G XP_011542192.1:n.368+63A>G
NM_000397.4:c.674+63A>G MANE Select NP_000388.2:n.674+63A>G