Canonical Allele Identifier: CA2618924978
Gene: KRT6B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52451588del , CM000674.2:g.52451588del GRCh38
NC_000012.11:g.52845372del , CM000674.1:g.52845372del GRCh37
NC_000012.10:g.51131639del NCBI36
NG_008299.1:g.5539del

Transcript Alleles

HGVS Amino-acid Change
ENST00000252252.4:c.491del MANE Select ENSP00000252252.3:p.Arg164LeufsTer21
ENST00000252252.3:c.491del ENSP00000252252.3:p.Arg164LeufsTer21
NM_005555.3:c.491del NP_005546.2:p.Arg164LeufsTer21
NM_005555.4:c.491del MANE Select NP_005546.2:p.Arg164LeufsTer21