Canonical Allele Identifier: CA725611860
Gene: CYBA HGNC NCBI

Linked Data

dbSNP Id: rs1467125346
gnomAD v3: 16-88643279-G-T
gnomAD v4: 16-88643279-G-T
MyVariant Identifiers: chr16:g.88709687G>T (hg19) chr16:g.88643279G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88643279G>T , CM000678.2:g.88643279G>T GRCh38
NC_000016.9:g.88709687G>T , CM000678.1:g.88709687G>T GRCh37
NC_000016.8:g.87237188G>T NCBI36
NG_007291.1:g.12771C>A , LRG_52:g.12771C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696156.1:c.*74C>A ENSP00000512446.1:n.*74C>A
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