Canonical Allele Identifier: CA2036500248
Gene: KRT6B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52451343G= , CM000674.2:g.52451343G= GRCh38
NC_000012.11:g.52845127G= , CM000674.1:g.52845127G= GRCh37
NC_000012.10:g.51131394G= NCBI36
NG_008299.1:g.5784C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252252.4:c.540+196C= MANE Select ENSP00000252252.3:n.540+196C=
ENST00000252252.3:c.540+196C= ENSP00000252252.3:n.540+196C=
NM_005555.3:c.540+196C= NP_005546.2:n.540+196C=
NM_005555.4:c.540+196C= MANE Select NP_005546.2:n.540+196C=