Canonical Allele Identifier: CA2637837966
Gene: KRT14 HGNC NCBI

Linked Data

gnomAD v4: 17-41586901-G-A
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.6:c.-67C>T ENSP00000167586.6:n.-67C>T
Search 100 bp 5'
Search 100 bp 3'