Canonical Allele Identifier: CA237279163
Gene: KRT4 HGNC NCBI

Linked Data

dbSNP Id: rs995024899
MyVariant Identifiers: chr12:g.53208149C>G (hg19) chr12:g.52814365C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814365C>G , CM000674.2:g.52814365C>G GRCh38
NC_000012.11:g.53208149C>G , CM000674.1:g.53208149C>G GRCh37
NC_000012.10:g.51494416C>G NCBI36
NG_007380.1:g.5187G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-307G>C ENSP00000448220.1:n.-307G>C
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