Canonical Allele Identifier: CA689878140
Gene: KRT4 HGNC NCBI

Linked Data

dbSNP Id: rs1341662968
gnomAD v3: 12-52814367-C-T
gnomAD v4: 12-52814367-C-T
MyVariant Identifiers: chr12:g.53208151C>T (hg19) chr12:g.52814367C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814367C>T , CM000674.2:g.52814367C>T GRCh38
NC_000012.11:g.53208151C>T , CM000674.1:g.53208151C>T GRCh37
NC_000012.10:g.51494418C>T NCBI36
NG_007380.1:g.5185G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-309G>A ENSP00000448220.1:n.-309G>A
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