Canonical Allele Identifier: CA2795998572

Gene: KRT6B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52451387del , CM000674.2:g.52451387del	GRCh38
NC_000012.11:g.52845171del , CM000674.1:g.52845171del	GRCh37
NC_000012.10:g.51131438del	NCBI36
NG_008299.1:g.5740del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252252.4:c.540+152del MANE Select	ENSP00000252252.3:n.540+152del
ENST00000252252.3:c.540+152del	ENSP00000252252.3:n.540+152del
NM_005555.3:c.540+152del	NP_005546.2:n.540+152del
NM_005555.4:c.540+152del MANE Select	NP_005546.2:n.540+152del