Canonical Allele Identifier: CA2036663698
Gene: KRT4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814327A= , CM000674.2:g.52814327A= GRCh38
NC_000012.11:g.53208111A= , CM000674.1:g.53208111A= GRCh37
NC_000012.10:g.51494378A= NCBI36
NG_007380.1:g.5225T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-269T= ENSP00000448220.1:n.-269T=