Canonical Allele Identifier: CA2260087103
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs2151398877
gnomAD v4: 17-41586906-G-A
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.6:c.-72C>T ENSP00000167586.6:n.-72C>T
Search 100 bp 5'
Search 100 bp 3'