Canonical Allele Identifier: CA2637837985
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586915G>T , CM000679.2:g.41586915G>T GRCh38
NC_000017.10:g.39743167G>T , CM000679.1:g.39743167G>T GRCh37
NC_000017.9:g.36996693G>T NCBI36
NG_008624.1:g.4981C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.6:c.-81C>A ENSP00000167586.6:n.-81C>A