Canonical Allele Identifier: CA689878083
Gene: KRT4 HGNC NCBI

Linked Data

dbSNP Id: rs1477905445
gnomAD v3: 12-52814320-C-T
gnomAD v4: 12-52814320-C-T
MyVariant Identifiers: chr12:g.53208104C>T (hg19) chr12:g.52814320C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814320C>T , CM000674.2:g.52814320C>T GRCh38
NC_000012.11:g.53208104C>T , CM000674.1:g.53208104C>T GRCh37
NC_000012.10:g.51494371C>T NCBI36
NG_007380.1:g.5232G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-262G>A ENSP00000448220.1:n.-262G>A
Search 100 bp 5'
Search 100 bp 3'