Canonical Allele Identifier: CA725611869
Gene: CYBA HGNC NCBI

Linked Data

dbSNP Id: rs888097899
gnomAD v3: 16-88643284-C-G
gnomAD v4: 16-88643284-C-G
MyVariant Identifiers: chr16:g.88709692C>G (hg19) chr16:g.88643284C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88643284C>G , CM000678.2:g.88643284C>G GRCh38
NC_000016.9:g.88709692C>G , CM000678.1:g.88709692C>G GRCh37
NC_000016.8:g.87237193C>G NCBI36
NG_007291.1:g.12766G>C , LRG_52:g.12766G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696156.1:c.*69G>C ENSP00000512446.1:n.*69G>C
ENST00000261623.7:c.*69G>C ENSP00000261623.3:n.*69G>C
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