Canonical Allele Identifier: CA384934727
Gene: KRT6C HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52863485A>G (hg19) chr12:g.52469701A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52469701A>G , CM000674.2:g.52469701A>G GRCh38
NC_000012.11:g.52863485A>G , CM000674.1:g.52863485A>G GRCh37
NC_000012.10:g.51149752A>G NCBI36
NG_012416.1:g.9085T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000252250.7:c.1393T>C MANE Select ENSP00000252250.6:p.Tyr465His
ENST00000252250.6:c.1393T>C ENSP00000252250.6:p.Tyr465His
NM_173086.4:c.1393T>C NP_775109.2:p.Tyr465His
NM_173086.5:c.1393T>C MANE Select NP_775109.2:p.Tyr465His
Search 100 bp 5'
Search 100 bp 3'