Canonical Allele Identifier: CA2637837974
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586904A>G , CM000679.2:g.41586904A>G GRCh38
NC_000017.10:g.39743156A>G , CM000679.1:g.39743156A>G GRCh37
NC_000017.9:g.36996682A>G NCBI36
NG_008624.1:g.4992T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.6:c.-70T>C ENSP00000167586.6:n.-70T>C