Canonical Allele Identifier: CA2036493648
Gene: KRT6B HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52447637T= , CM000674.2:g.52447637T= GRCh38
NC_000012.11:g.52841421T= , CM000674.1:g.52841421T= GRCh37
NC_000012.10:g.51127688T= NCBI36
NG_008299.1:g.9490A=

Transcript Alleles

HGVS Amino-acid change
ENST00000252252.4:c.1425-64A= MANE Select ENSP00000252252.3:n.1425-64A=
ENST00000252252.3:c.1425-64A= ENSP00000252252.3:n.1425-64A=
NM_005555.3:c.1425-64A= NP_005546.2:n.1425-64A=
NM_005555.4:c.1425-64A= MANE Select NP_005546.2:n.1425-64A=
Search 100 bp 5'
Search 100 bp 3'