Canonical Allele Identifier: CA237279199
Gene: KRT4 HGNC NCBI

Linked Data

dbSNP Id: rs537631692
gnomAD v2: 12-53208199-G-A
gnomAD v3: 12-52814415-G-A
gnomAD v4: 12-52814415-G-A
MyVariant Identifiers: chr12:g.53208199G>A (hg19) chr12:g.52814415G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814415G>A , CM000674.2:g.52814415G>A GRCh38
NC_000012.11:g.53208199G>A , CM000674.1:g.53208199G>A GRCh37
NC_000012.10:g.51494466G>A NCBI36
NG_007380.1:g.5137C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-357C>T ENSP00000448220.1:n.-357C>T
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