Canonical Allele Identifier: CA2618968299
Gene: KRT4 HGNC NCBI

Linked Data

gnomAD v4: 12-52814362-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814362A>C , CM000674.2:g.52814362A>C GRCh38
NC_000012.11:g.53208146A>C , CM000674.1:g.53208146A>C GRCh37
NC_000012.10:g.51494413A>C NCBI36
NG_007380.1:g.5190T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-304T>G ENSP00000448220.1:n.-304T>G
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