Canonical Allele Identifier: CA2036492688
Gene: KRT6C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52469607G= , CM000674.2:g.52469607G= GRCh38
NC_000012.11:g.52863391G= , CM000674.1:g.52863391G= GRCh37
NC_000012.10:g.51149658G= NCBI36
NG_012416.1:g.9179C=

Transcript Alleles

HGVS Amino-acid change
ENST00000252250.7:c.1424+63C= MANE Select ENSP00000252250.6:n.1424+63C=
ENST00000252250.6:c.1424+63C= ENSP00000252250.6:n.1424+63C=
NM_173086.4:c.1424+63C= NP_775109.2:n.1424+63C=
NM_173086.5:c.1424+63C= MANE Select NP_775109.2:n.1424+63C=
Search 100 bp 5'
Search 100 bp 3'