Canonical Allele Identifier: CA237279201
Gene: KRT4 HGNC NCBI

Linked Data

dbSNP Id: rs1024726045
gnomAD v4: 12-52814419-G-A
MyVariant Identifiers: chr12:g.53208203G>A (hg19) chr12:g.52814419G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814419G>A , CM000674.2:g.52814419G>A GRCh38
NC_000012.11:g.53208203G>A , CM000674.1:g.53208203G>A GRCh37
NC_000012.10:g.51494470G>A NCBI36
NG_007380.1:g.5133C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-361C>T ENSP00000448220.1:n.-361C>T
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