Canonical Allele Identifier: CA2504615687

Gene: KRT6B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52451377C>G , CM000674.2:g.52451377C>G	GRCh38
NC_000012.11:g.52845161C>G , CM000674.1:g.52845161C>G	GRCh37
NC_000012.10:g.51131428C>G	NCBI36
NG_008299.1:g.5750G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252252.4:c.540+162G>C MANE Select	ENSP00000252252.3:n.540+162G>C
ENST00000252252.3:c.540+162G>C	ENSP00000252252.3:n.540+162G>C
NM_005555.3:c.540+162G>C	NP_005546.2:n.540+162G>C
NM_005555.4:c.540+162G>C MANE Select	NP_005546.2:n.540+162G>C