Canonical Allele Identifier: CA2036663671
Gene: KRT4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814260A= , CM000674.2:g.52814260A= GRCh38
NC_000012.11:g.53208044A= , CM000674.1:g.53208044A= GRCh37
NC_000012.10:g.51494311A= NCBI36
NG_007380.1:g.5292T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-202T= ENSP00000448220.1:n.-202T=