Canonical Allele Identifier: CA2618967800
Gene: KRT4 HGNC NCBI

Linked Data

gnomAD v4: 12-52814161-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814161G>A , CM000674.2:g.52814161G>A GRCh38
NC_000012.11:g.53207945G>A , CM000674.1:g.53207945G>A GRCh37
NC_000012.10:g.51494212G>A NCBI36
NG_007380.1:g.5391C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-103C>T ENSP00000448220.1:n.-103C>T
Search 100 bp 5'
Search 100 bp 3'