Canonical Allele Identifier: CA2618968428
Gene: KRT4 HGNC NCBI

Linked Data

gnomAD v4: 12-52814421-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814421C>T , CM000674.2:g.52814421C>T GRCh38
NC_000012.11:g.53208205C>T , CM000674.1:g.53208205C>T GRCh37
NC_000012.10:g.51494472C>T NCBI36
NG_007380.1:g.5131G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-363G>A ENSP00000448220.1:n.-363G>A
Search 100 bp 5'
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