Canonical Allele Identifier: CA286347996
Gene: CYBA HGNC NCBI

Linked Data

dbSNP Id: rs1036593520
gnomAD v3: 16-88643288-C-T
gnomAD v4: 16-88643288-C-T
MyVariant Identifiers: chr16:g.88709696C>T (hg19) chr16:g.88643288C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88643288C>T , CM000678.2:g.88643288C>T GRCh38
NC_000016.9:g.88709696C>T , CM000678.1:g.88709696C>T GRCh37
NC_000016.8:g.87237197C>T NCBI36
NG_007291.1:g.12762G>A , LRG_52:g.12762G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696156.1:c.*65G>A ENSP00000512446.1:n.*65G>A
ENST00000261623.7:c.*65G>A ENSP00000261623.3:n.*65G>A
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