Canonical Allele Identifier: CA2260087106
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586909A= , CM000679.2:g.41586909A= GRCh38
NC_000017.10:g.39743161A= , CM000679.1:g.39743161A= GRCh37
NC_000017.9:g.36996687A= NCBI36
NG_008624.1:g.4987T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.6:c.-75T= ENSP00000167586.6:n.-75T=