Canonical Allele Identifier: CA290665694
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs1030370228

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586906G>C , CM000679.2:g.41586906G>C GRCh38
NC_000017.10:g.39743158G>C , CM000679.1:g.39743158G>C GRCh37
NC_000017.9:g.36996684G>C NCBI36
NG_008624.1:g.4990C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.6:c.-72C>G ENSP00000167586.6:n.-72C>G