Canonical Allele Identifier: CA515673967
Gene: CYBB HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.37663132G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37803879G>A , CM000685.2:g.37803879G>A GRCh38
NC_000023.10:g.37663132G>A , CM000685.1:g.37663132G>A GRCh37
NC_000023.9:g.37548076G>A NCBI36
NG_009065.1:g.28863G>A , LRG_53:g.28863G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696170.1:c.*409G>A ENSP00000512461.1:n.*409G>A
ENST00000696171.1:c.804G>A ENSP00000512462.1:p.Val268=
ENST00000378588.5:c.900G>A MANE Select ENSP00000367851.4:p.Val300=
ENST00000378588.4:c.900G>A ENSP00000367851.4:p.Val300=
ENST00000465127.1:c.171+377879G>A ENSP00000417050.1:n.171+377879G>A
ENST00000492288.1:n.325G>A
NM_000397.3:c.900G>A , LRG_53t1:c.900G>A NP_000388.2:p.Val300=
XM_011543890.1:c.594G>A XP_011542192.1:p.Val198=
NM_000397.4:c.900G>A MANE Select NP_000388.2:p.Val300=
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