Canonical Allele Identifier: CA2036500208
Gene: KRT6B HGNC NCBI

Linked Data

dbSNP Id: rs1940398828

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52451320del , CM000674.2:g.52451320del GRCh38
NC_000012.11:g.52845104del , CM000674.1:g.52845104del GRCh37
NC_000012.10:g.51131371del NCBI36
NG_008299.1:g.5807del

Transcript Alleles

HGVS Amino-acid Change
ENST00000252252.4:c.540+219del MANE Select ENSP00000252252.3:n.540+219del
ENST00000252252.3:c.540+219del ENSP00000252252.3:n.540+219del
NM_005555.3:c.540+219del NP_005546.2:n.540+219del
NM_005555.4:c.540+219del MANE Select NP_005546.2:n.540+219del