Canonical Allele Identifier: CA412977602
Gene: CYBB HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.37664257A>T (hg19) chrX:g.37805004A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37805004A>T , CM000685.2:g.37805004A>T GRCh38
NC_000023.10:g.37664257A>T , CM000685.1:g.37664257A>T GRCh37
NC_000023.9:g.37549201A>T NCBI36
NG_009065.1:g.29988A>T , LRG_53:g.29988A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696170.1:c.*661-2A>T ENSP00000512461.1:n.*661-2A>T
ENST00000696171.1:c.1056-2A>T ENSP00000512462.1:n.1056-2A>T
ENST00000378588.5:c.1152-2A>T MANE Select ENSP00000367851.4:n.1152-2A>T
ENST00000378588.4:c.1152-2A>T ENSP00000367851.4:n.1152-2A>T
ENST00000465127.1:c.171+379004A>T ENSP00000417050.1:n.171+379004A>T
NM_000397.3:c.1152-2A>T , LRG_53t1:c.1152-2A>T NP_000388.2:n.1152-2A>T
XM_011543890.1:c.846-2A>T XP_011542192.1:n.846-2A>T
NM_000397.4:c.1152-2A>T MANE Select NP_000388.2:n.1152-2A>T
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