Canonical Allele Identifier: CA290665696
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs554230769 rs2151398884
gnomAD v2: 17-39743165-G-A
gnomAD v3: 17-41586913-G-A
gnomAD v4: 17-41586913-G-A
MyVariant Identifiers: chr17:g.39743165G>A (hg19) chr17:g.41586913G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586913G>A , CM000679.2:g.41586913G>A GRCh38
NC_000017.10:g.39743165G>A , CM000679.1:g.39743165G>A GRCh37
NC_000017.9:g.36996691G>A NCBI36
NG_008624.1:g.4983C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.6:c.-79C>T ENSP00000167586.6:n.-79C>T
Search 100 bp 5'
Search 100 bp 3'