Canonical Allele Identifier: CA515670852
Gene: CYBB HGNC NCBI

Linked Data

gnomAD v4: X-37795995-C-T
MyVariant Identifiers: chrX:g.37655248C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37795995C>T , CM000685.2:g.37795995C>T GRCh38
NC_000023.10:g.37655248C>T , CM000685.1:g.37655248C>T GRCh37
NC_000023.9:g.37540188C>T NCBI36
NG_009065.1:g.20975C>T , LRG_53:g.20975C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000696170.1:c.*37C>T ENSP00000512461.1:n.*37C>T
ENST00000696171.1:c.432C>T ENSP00000512462.1:p.Gly144=
ENST00000696172.1:c.338-2960C>T ENSP00000512463.1:n.338-2960C>T
ENST00000378588.5:c.528C>T MANE Select ENSP00000367851.4:p.Gly176=
ENST00000378588.4:c.528C>T ENSP00000367851.4:p.Gly176=
ENST00000465127.1:c.171+369995C>T ENSP00000417050.1:n.171+369995C>T
NM_000397.3:c.528C>T , LRG_53t1:c.528C>T NP_000388.2:p.Gly176=
XM_011543890.1:c.222C>T XP_011542192.1:p.Gly74=
NM_000397.4:c.528C>T MANE Select NP_000388.2:p.Gly176=