Canonical Allele Identifier: CA2637837975
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

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