Canonical Allele Identifier: CA515677641
Gene: CYBB HGNC NCBI

Linked Data

gnomAD v4: X-37805081-A-C
MyVariant Identifiers: chrX:g.37664334A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37805081A>C , CM000685.2:g.37805081A>C GRCh38
NC_000023.10:g.37664334A>C , CM000685.1:g.37664334A>C GRCh37
NC_000023.9:g.37549278A>C NCBI36
NG_009065.1:g.30065A>C , LRG_53:g.30065A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696170.1:c.*736A>C ENSP00000512461.1:n.*736A>C
ENST00000696171.1:c.1131A>C ENSP00000512462.1:p.Ala377=
ENST00000378588.5:c.1227A>C MANE Select ENSP00000367851.4:p.Ala409=
ENST00000378588.4:c.1227A>C ENSP00000367851.4:p.Ala409=
ENST00000465127.1:c.171+379081A>C ENSP00000417050.1:n.171+379081A>C
NM_000397.3:c.1227A>C , LRG_53t1:c.1227A>C NP_000388.2:p.Ala409=
XM_011543890.1:c.921A>C XP_011542192.1:p.Ala307=
NM_000397.4:c.1227A>C MANE Select NP_000388.2:p.Ala409=
Search 100 bp 5'
Search 100 bp 3'