Canonical Allele Identifier: CA875138867
Gene: CYBB HGNC NCBI

Linked Data

dbSNP Id: rs1209296710
MyVariant Identifiers: chrX:g.37804924C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37804924C>A , CM000685.2:g.37804924C>A GRCh38
NC_000023.10:g.37664177C>A , CM000685.1:g.37664177C>A GRCh37
NC_000023.9:g.37549121C>A NCBI36
NG_009065.1:g.29908C>A , LRG_53:g.29908C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696170.1:c.*661-82C>A ENSP00000512461.1:n.*661-82C>A
ENST00000696171.1:c.1056-82C>A ENSP00000512462.1:n.1056-82C>A
ENST00000378588.5:c.1152-82C>A MANE Select ENSP00000367851.4:n.1152-82C>A
ENST00000378588.4:c.1152-82C>A ENSP00000367851.4:n.1152-82C>A
ENST00000465127.1:c.171+378924C>A ENSP00000417050.1:n.171+378924C>A
NM_000397.3:c.1152-82C>A , LRG_53t1:c.1152-82C>A NP_000388.2:n.1152-82C>A
XM_011543890.1:c.846-82C>A XP_011542192.1:n.846-82C>A
NM_000397.4:c.1152-82C>A MANE Select NP_000388.2:n.1152-82C>A
Search 100 bp 5'
Search 100 bp 3'