Canonical Allele Identifier: CA619230762
Gene: HYKK HGNC NCBI

Linked Data

dbSNP Id: rs1377675334
gnomAD v2: 15-78826955-A-C
gnomAD v3: 15-78534613-A-C
gnomAD v4: 15-78534613-A-C
MyVariant Identifiers: chr15:g.78826955A>C (hg19) chr15:g.78534613A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78534613A>C , CM000677.2:g.78534613A>C GRCh38
NC_000015.9:g.78826955A>C , CM000677.1:g.78826955A>C GRCh37
NC_000015.8:g.76614010A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000388988.9:c.*943A>C MANE Select ENSP00000373640.4:n.*943A>C
ENST00000408962.6:c.662-2687A>C ENSP00000386197.2:n.662-2687A>C
ENST00000563233.2:c.662-2687A>C ENSP00000454850.1:n.662-2687A>C
ENST00000569878.5:c.2065A>C ENSP00000455459.1:n.2065A>C
NM_001083612.1:c.662-2687A>C NP_001077081.1:n.662-2687A>C
NM_001013619.3:c.*943A>C NP_001013641.2:n.*943A>C
NM_001013619.4:c.*943A>C MANE Select NP_001013641.2:n.*943A>C
NM_001083612.2:c.662-2687A>C NP_001077081.1:n.662-2687A>C
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