Canonical Allele Identifier: CA2618968269
Gene: KRT4 HGNC NCBI

Linked Data

gnomAD v4: 12-52814351-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814351T>C , CM000674.2:g.52814351T>C GRCh38
NC_000012.11:g.53208135T>C , CM000674.1:g.53208135T>C GRCh37
NC_000012.10:g.51494402T>C NCBI36
NG_007380.1:g.5201A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-293A>G ENSP00000448220.1:n.-293A>G
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