Canonical Allele Identifier: CA2739419902
Gene: KRT4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814190A>T , CM000674.2:g.52814190A>T GRCh38
NC_000012.11:g.53207974A>T , CM000674.1:g.53207974A>T GRCh37
NC_000012.10:g.51494241A>T NCBI36
NG_007380.1:g.5362T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-132T>A ENSP00000448220.1:n.-132T>A