Canonical Allele Identifier: CA2618968413
Gene: KRT4 HGNC NCBI

Linked Data

gnomAD v4: 12-52814417-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814417T>G , CM000674.2:g.52814417T>G GRCh38
NC_000012.11:g.53208201T>G , CM000674.1:g.53208201T>G GRCh37
NC_000012.10:g.51494468T>G NCBI36
NG_007380.1:g.5135A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-359A>C ENSP00000448220.1:n.-359A>C
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