Canonical Allele Identifier: CA2637837971
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586903A>T , CM000679.2:g.41586903A>T GRCh38
NC_000017.10:g.39743155A>T , CM000679.1:g.39743155A>T GRCh37
NC_000017.9:g.36996681A>T NCBI36
NG_008624.1:g.4993T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.6:c.-69T>A ENSP00000167586.6:n.-69T>A