Canonical Allele Identifier: CA689878144
Gene: KRT4 HGNC NCBI

Linked Data

dbSNP Id: rs1334072328
gnomAD v3: 12-52814372-T-A
gnomAD v4: 12-52814372-T-A
MyVariant Identifiers: chr12:g.53208156T>A (hg19) chr12:g.52814372T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814372T>A , CM000674.2:g.52814372T>A GRCh38
NC_000012.11:g.53208156T>A , CM000674.1:g.53208156T>A GRCh37
NC_000012.10:g.51494423T>A NCBI36
NG_007380.1:g.5180A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-314A>T ENSP00000448220.1:n.-314A>T
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