Canonical Allele Identifier: CA2036663680
Gene: KRT4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814289C= , CM000674.2:g.52814289C= GRCh38
NC_000012.11:g.53208073C= , CM000674.1:g.53208073C= GRCh37
NC_000012.10:g.51494340C= NCBI36
NG_007380.1:g.5263G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-231G= ENSP00000448220.1:n.-231G=