Canonical Allele Identifier: CA772039848
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs1237667318
gnomAD v4: 17-41584438-A-G
MyVariant Identifiers: chr17:g.39740690A>G (hg19) chr17:g.41584438A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584438A>G , CM000679.2:g.41584438A>G GRCh38
NC_000017.10:g.39740690A>G , CM000679.1:g.39740690A>G GRCh37
NC_000017.9:g.36994216A>G NCBI36
NG_008624.1:g.7458T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.609-25T>C MANE Select ENSP00000167586.6:n.609-25T>C
ENST00000167586.6:c.609-25T>C ENSP00000167586.6:n.609-25T>C
ENST00000476662.1:n.34T>C
NM_000526.4:c.609-25T>C NP_000517.2:n.609-25T>C
NM_000526.5:c.609-25T>C MANE Select NP_000517.3:n.609-25T>C
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