Canonical Allele Identifier: CA2036500989
Gene: KRT6B HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52451697G= , CM000674.2:g.52451697G= GRCh38
NC_000012.11:g.52845481G= , CM000674.1:g.52845481G= GRCh37
NC_000012.10:g.51131748G= NCBI36
NG_008299.1:g.5430C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252252.4:c.382C= MANE Select ENSP00000252252.3:p.Pro128=
ENST00000252252.3:c.382C= ENSP00000252252.3:p.Pro128=
NM_005555.3:c.382C= NP_005546.2:p.Pro128=
NM_005555.4:c.382C= MANE Select NP_005546.2:p.Pro128=
Search 100 bp 5'
Search 100 bp 3'