Canonical Allele Identifier: CA2637837967
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586901G>C , CM000679.2:g.41586901G>C GRCh38
NC_000017.10:g.39743153G>C , CM000679.1:g.39743153G>C GRCh37
NC_000017.9:g.36996679G>C NCBI36
NG_008624.1:g.4995C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.6:c.-67C>G ENSP00000167586.6:n.-67C>G