Canonical Allele Identifier: CA2036663629
Gene: KRT4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814162G= , CM000674.2:g.52814162G= GRCh38
NC_000012.11:g.53207946G= , CM000674.1:g.53207946G= GRCh37
NC_000012.10:g.51494213G= NCBI36
NG_007380.1:g.5390C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-104C= ENSP00000448220.1:n.-104C=