Canonical Allele Identifier: CA2189568060
Gene: HYKK HGNC NCBI

Linked Data

dbSNP Id: rs2052345260
gnomAD v4: 15-78534608-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78534608T>C , CM000677.2:g.78534608T>C GRCh38
NC_000015.9:g.78826950T>C , CM000677.1:g.78826950T>C GRCh37
NC_000015.8:g.76614005T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000388988.9:c.*938T>C MANE Select ENSP00000373640.4:n.*938T>C
ENST00000408962.6:c.662-2692T>C ENSP00000386197.2:n.662-2692T>C
ENST00000563233.2:c.662-2692T>C ENSP00000454850.1:n.662-2692T>C
ENST00000569878.5:c.2060T>C ENSP00000455459.1:n.2060T>C
NM_001083612.1:c.662-2692T>C NP_001077081.1:n.662-2692T>C
NM_001013619.3:c.*938T>C NP_001013641.2:n.*938T>C
NM_001013619.4:c.*938T>C MANE Select NP_001013641.2:n.*938T>C
NM_001083612.2:c.662-2692T>C NP_001077081.1:n.662-2692T>C
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