Canonical Allele Identifier: CA2637837968
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586902G>A , CM000679.2:g.41586902G>A GRCh38
NC_000017.10:g.39743154G>A , CM000679.1:g.39743154G>A GRCh37
NC_000017.9:g.36996680G>A NCBI36
NG_008624.1:g.4994C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.6:c.-68C>T ENSP00000167586.6:n.-68C>T