Canonical Allele Identifier: CA2618968448
Gene: KRT4 HGNC NCBI

Linked Data

gnomAD v4: 12-52814431-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814431C>G , CM000674.2:g.52814431C>G GRCh38
NC_000012.11:g.53208215C>G , CM000674.1:g.53208215C>G GRCh37
NC_000012.10:g.51494482C>G NCBI36
NG_007380.1:g.5121G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-373G>C ENSP00000448220.1:n.-373G>C
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