Canonical Allele Identifier: CA2795998561

Gene: KRT6B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52451320T>G , CM000674.2:g.52451320T>G	GRCh38
NC_000012.11:g.52845104T>G , CM000674.1:g.52845104T>G	GRCh37
NC_000012.10:g.51131371T>G	NCBI36
NG_008299.1:g.5807A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252252.4:c.540+219A>C MANE Select	ENSP00000252252.3:n.540+219A>C
ENST00000252252.3:c.540+219A>C	ENSP00000252252.3:n.540+219A>C
NM_005555.3:c.540+219A>C	NP_005546.2:n.540+219A>C
NM_005555.4:c.540+219A>C MANE Select	NP_005546.2:n.540+219A>C