Canonical Allele Identifier: CA2637837977
Gene: KRT14 HGNC NCBI

Linked Data

gnomAD v4: 17-41586908-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586908G>T , CM000679.2:g.41586908G>T GRCh38
NC_000017.10:g.39743160G>T , CM000679.1:g.39743160G>T GRCh37
NC_000017.9:g.36996686G>T NCBI36
NG_008624.1:g.4988C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.6:c.-74C>A ENSP00000167586.6:n.-74C>A
Search 100 bp 5'
Search 100 bp 3'