Canonical Allele Identifier: CA2260087102
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586906G= , CM000679.2:g.41586906G= GRCh38
NC_000017.10:g.39743158G= , CM000679.1:g.39743158G= GRCh37
NC_000017.9:g.36996684G= NCBI36
NG_008624.1:g.4990C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.6:c.-72C= ENSP00000167586.6:n.-72C=