Canonical Allele Identifier: CA619230761
Gene: HYKK HGNC NCBI

Linked Data

dbSNP Id: rs1456969642
gnomAD v2: 15-78826886-C-A
gnomAD v3: 15-78534544-C-A
gnomAD v4: 15-78534544-C-A
MyVariant Identifiers: chr15:g.78826886C>A (hg19) chr15:g.78534544C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78534544C>A , CM000677.2:g.78534544C>A GRCh38
NC_000015.9:g.78826886C>A , CM000677.1:g.78826886C>A GRCh37
NC_000015.8:g.76613941C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000388988.9:c.*874C>A MANE Select ENSP00000373640.4:n.*874C>A
ENST00000408962.6:c.662-2756C>A ENSP00000386197.2:n.662-2756C>A
ENST00000563233.2:c.662-2756C>A ENSP00000454850.1:n.662-2756C>A
ENST00000569878.5:c.1996C>A ENSP00000455459.1:n.1996C>A
NM_001083612.1:c.662-2756C>A NP_001077081.1:n.662-2756C>A
NM_001013619.3:c.*874C>A NP_001013641.2:n.*874C>A
NM_001013619.4:c.*874C>A MANE Select NP_001013641.2:n.*874C>A
NM_001083612.2:c.662-2756C>A NP_001077081.1:n.662-2756C>A
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