Canonical Allele Identifier: CA2260087104
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586907G= , CM000679.2:g.41586907G= GRCh38
NC_000017.10:g.39743159G= , CM000679.1:g.39743159G= GRCh37
NC_000017.9:g.36996685G= NCBI36
NG_008624.1:g.4989C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.6:c.-73C= ENSP00000167586.6:n.-73C=