Canonical Allele Identifier: CA772039903
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs1260848124
gnomAD v3: 17-41584633-G-A
gnomAD v4: 17-41584633-G-A
MyVariant Identifiers: chr17:g.39740885G>A (hg19) chr17:g.41584633G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584633G>A , CM000679.2:g.41584633G>A GRCh38
NC_000017.10:g.39740885G>A , CM000679.1:g.39740885G>A GRCh37
NC_000017.9:g.36994411G>A NCBI36
NG_008624.1:g.7263C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.609-220C>T MANE Select ENSP00000167586.6:n.609-220C>T
ENST00000167586.6:c.609-220C>T ENSP00000167586.6:n.609-220C>T
NM_000526.4:c.609-220C>T NP_000517.2:n.609-220C>T
NM_000526.5:c.609-220C>T MANE Select NP_000517.3:n.609-220C>T
Search 100 bp 5'
Search 100 bp 3'