Canonical Allele Identifier: CA2036663721
Gene: KRT4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814388G= , CM000674.2:g.52814388G= GRCh38
NC_000012.11:g.53208172G= , CM000674.1:g.53208172G= GRCh37
NC_000012.10:g.51494439G= NCBI36
NG_007380.1:g.5164C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-330C= ENSP00000448220.1:n.-330C=