Canonical Allele Identifier: CA2739420019
Gene: KRT4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814264A>T , CM000674.2:g.52814264A>T GRCh38
NC_000012.11:g.53208048A>T , CM000674.1:g.53208048A>T GRCh37
NC_000012.10:g.51494315A>T NCBI36
NG_007380.1:g.5288T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-206T>A ENSP00000448220.1:n.-206T>A