Canonical Allele Identifier: CA2036493866
Gene: KRT6B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52447742A= , CM000674.2:g.52447742A= GRCh38
NC_000012.11:g.52841526A= , CM000674.1:g.52841526A= GRCh37
NC_000012.10:g.51127793A= NCBI36
NG_008299.1:g.9385T=

Transcript Alleles

HGVS Amino-acid change
ENST00000252252.4:c.1424+36T= MANE Select ENSP00000252252.3:n.1424+36T=
ENST00000252252.3:c.1424+36T= ENSP00000252252.3:n.1424+36T=
NM_005555.3:c.1424+36T= NP_005546.2:n.1424+36T=
NM_005555.4:c.1424+36T= MANE Select NP_005546.2:n.1424+36T=