Canonical Allele Identifier: CA654742182

Gene: KRT6B

Linked Data

• COSMIC: COSN24794631

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52447683A>C , CM000674.2:g.52447683A>C	GRCh38
NC_000012.11:g.52841467A>C , CM000674.1:g.52841467A>C	GRCh37
NC_000012.10:g.51127734A>C	NCBI36
NG_008299.1:g.9444T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000252252.4:c.1424+95T>G MANE Select	ENSP00000252252.3:n.1424+95T>G
ENST00000252252.3:c.1424+95T>G	ENSP00000252252.3:n.1424+95T>G
NM_005555.3:c.1424+95T>G	NP_005546.2:n.1424+95T>G
NM_005555.4:c.1424+95T>G MANE Select	NP_005546.2:n.1424+95T>G