Canonical Allele Identifier: CA273904035
Gene: HYKK HGNC NCBI
MyVariant.info:
GRCh38 chr15:g.78533838G>A
GRCh37 chr15:g.78826180G>A
gnomAD v2:
15:78826180 G / A
gnomAD v3:
15:78533838 G / A
gnomAD v4:
chr15-78533838-G-A
Joint Max Group AF 0.75666949 (AMR)
Genomes Max Group AF 0.74653447 (AFR)
Exomes Max Group AF 0.76588932 (AMR)
dbSNP:
931794
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78533838G>A , CM000677.2:g.78533838G>A GRCh38
NC_000015.9:g.78826180G>A , CM000677.1:g.78826180G>A GRCh37
NC_000015.8:g.76613235G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000388988.9:c.*168G>A MANE Select ENSP00000373640.4:n.*168G>A
ENST00000408962.6:c.662-3462G>A ENSP00000386197.2:n.662-3462G>A
ENST00000563233.2:c.662-3462G>A ENSP00000454850.1:n.662-3462G>A
ENST00000569878.5:c.1290G>A ENSP00000455459.1:n.1290G>A
NM_001083612.1:c.662-3462G>A NP_001077081.1:n.662-3462G>A
NM_001013619.3:c.*168G>A NP_001013641.2:n.*168G>A
NM_001013619.4:c.*168G>A MANE Select NP_001013641.2:n.*168G>A
NM_001083612.2:c.662-3462G>A NP_001077081.1:n.662-3462G>A
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