Canonical Allele Identifier: CA626215406
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs372692465
gnomAD v2: 17-39740207-T-C
gnomAD v4: 17-41583955-T-C
MyVariant Identifiers: chr17:g.39740207T>C (hg19) chr17:g.41583955T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583955T>C , CM000679.2:g.41583955T>C GRCh38
NC_000017.10:g.39740207T>C , CM000679.1:g.39740207T>C GRCh37
NC_000017.9:g.36993733T>C NCBI36
NG_008624.1:g.7941A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.766-34A>G MANE Select ENSP00000167586.6:n.766-34A>G
ENST00000167586.6:c.766-34A>G ENSP00000167586.6:n.766-34A>G
ENST00000476662.1:n.216-34A>G
NM_000526.4:c.766-34A>G NP_000517.2:n.766-34A>G
NM_000526.5:c.766-34A>G MANE Select NP_000517.3:n.766-34A>G
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