Canonical Allele Identifier: CA2260087108
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586912C= , CM000679.2:g.41586912C= GRCh38
NC_000017.10:g.39743164C= , CM000679.1:g.39743164C= GRCh37
NC_000017.9:g.36996690C= NCBI36
NG_008624.1:g.4984G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.6:c.-78G= ENSP00000167586.6:n.-78G=