Canonical Allele Identifier: CA8562512
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs201736303
ExAC: 17:39739748 G / A
gnomAD v2: 17-39739748-G-A
gnomAD v3: 17-41583496-G-A
gnomAD v4: 17-41583496-G-A
MyVariant Identifiers: chr17:g.39739748G>A (hg19) chr17:g.41583496G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583496G>A , CM000679.2:g.41583496G>A GRCh38
NC_000017.10:g.39739748G>A , CM000679.1:g.39739748G>A GRCh37
NC_000017.9:g.36993274G>A NCBI36
NG_008624.1:g.8400C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.1054-41C>T MANE Select ENSP00000167586.6:n.1054-41C>T
ENST00000167586.6:c.1054-41C>T ENSP00000167586.6:n.1054-41C>T
ENST00000476662.1:n.504-41C>T
NM_000526.4:c.1054-41C>T NP_000517.2:n.1054-41C>T
NM_000526.5:c.1054-41C>T MANE Select NP_000517.3:n.1054-41C>T
Search 100 bp 5'
Search 100 bp 3'