Canonical Allele Identifier: CA8562405
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs758226672
ExAC: 17:39739318 C / T
gnomAD v2: 17-39739318-C-T
gnomAD v3: 17-41583066-C-T
gnomAD v4: 17-41583066-C-T
MyVariant Identifiers: chr17:g.39739318C>T (hg19) chr17:g.41583066C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583066C>T , CM000679.2:g.41583066C>T GRCh38
NC_000017.10:g.39739318C>T , CM000679.1:g.39739318C>T GRCh37
NC_000017.9:g.36992844C>T NCBI36
NG_008624.1:g.8830G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.1321+28G>A MANE Select ENSP00000167586.6:n.1321+28G>A
ENST00000167586.6:c.1321+28G>A ENSP00000167586.6:n.1321+28G>A
ENST00000441550.2:n.296G>A
NM_000526.4:c.1321+28G>A NP_000517.2:n.1321+28G>A
NM_000526.5:c.1321+28G>A MANE Select NP_000517.3:n.1321+28G>A
Search 100 bp 5'
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