Canonical Allele Identifier: CA2618968359
Gene: KRT4 HGNC NCBI

Linked Data

gnomAD v4: 12-52814387-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814387A>G , CM000674.2:g.52814387A>G GRCh38
NC_000012.11:g.53208171A>G , CM000674.1:g.53208171A>G GRCh37
NC_000012.10:g.51494438A>G NCBI36
NG_007380.1:g.5165T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-329T>C ENSP00000448220.1:n.-329T>C
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