Canonical Allele Identifier: CA772039910
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs976674033
MyVariant Identifiers: chr17:g.39740892G>A (hg19) chr17:g.41584640G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584640G>A , CM000679.2:g.41584640G>A GRCh38
NC_000017.10:g.39740892G>A , CM000679.1:g.39740892G>A GRCh37
NC_000017.9:g.36994418G>A NCBI36
NG_008624.1:g.7256C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.609-227C>T MANE Select ENSP00000167586.6:n.609-227C>T
ENST00000167586.6:c.609-227C>T ENSP00000167586.6:n.609-227C>T
NM_000526.4:c.609-227C>T NP_000517.2:n.609-227C>T
NM_000526.5:c.609-227C>T MANE Select NP_000517.3:n.609-227C>T
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