Canonical Allele Identifier: CA2618968349
Gene: KRT4 HGNC NCBI

Linked Data

gnomAD v4: 12-52814384-T-TGGG
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814384_52814385insGGG , CM000674.2:g.52814384_52814385insGGG GRCh38
NC_000012.11:g.53208168_53208169insGGG , CM000674.1:g.53208168_53208169insGGG GRCh37
NC_000012.10:g.51494435_51494436insGGG NCBI36
NG_007380.1:g.5167_5168insCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-327_-326insCCC ENSP00000448220.1:n.-327_-326insCCC
Search 100 bp 5'
Search 100 bp 3'