Canonical Allele Identifier: CA605088149
Gene: KRT4 HGNC NCBI

Linked Data

dbSNP Id: rs1212532821
gnomAD v2: 12-53207948-C-T
gnomAD v4: 12-52814164-C-T
COSMIC: COSM4042938
MyVariant Identifiers: chr12:g.53207948C>T (hg19) chr12:g.52814164C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814164C>T , CM000674.2:g.52814164C>T GRCh38
NC_000012.11:g.53207948C>T , CM000674.1:g.53207948C>T GRCh37
NC_000012.10:g.51494215C>T NCBI36
NG_007380.1:g.5388G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-106G>A ENSP00000448220.1:n.-106G>A
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