Canonical Allele Identifier: CA2036663713
Gene: KRT4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814367C= , CM000674.2:g.52814367C= GRCh38
NC_000012.11:g.53208151C= , CM000674.1:g.53208151C= GRCh37
NC_000012.10:g.51494418C= NCBI36
NG_007380.1:g.5185G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-309G= ENSP00000448220.1:n.-309G=