Canonical Allele Identifier: CA2618968318
Gene: KRT4 HGNC NCBI

Linked Data

gnomAD v4: 12-52814370-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814370C>T , CM000674.2:g.52814370C>T GRCh38
NC_000012.11:g.53208154C>T , CM000674.1:g.53208154C>T GRCh37
NC_000012.10:g.51494421C>T NCBI36
NG_007380.1:g.5182G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-312G>A ENSP00000448220.1:n.-312G>A
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