Canonical Allele Identifier: CA399476583
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs1907415806
gnomAD v4: 17-41583607-C-G
MyVariant Identifiers: chr17:g.39739859C>G (hg19) chr17:g.41583607C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583607C>G , CM000679.2:g.41583607C>G GRCh38
NC_000017.10:g.39739859C>G , CM000679.1:g.39739859C>G GRCh37
NC_000017.9:g.36993385C>G NCBI36
NG_008624.1:g.8289G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.997G>C MANE Select ENSP00000167586.6:p.Glu333Gln
ENST00000167586.6:c.997G>C ENSP00000167586.6:p.Glu333Gln
ENST00000476662.1:n.447G>C
NM_000526.4:c.997G>C NP_000517.2:p.Glu333Gln
NM_000526.5:c.997G>C MANE Select NP_000517.3:p.Glu333Gln
Search 100 bp 5'
Search 100 bp 3'