Canonical Allele Identifier: CA2036493990

Gene: KRT6B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52447789G= , CM000674.2:g.52447789G=	GRCh38
NC_000012.11:g.52841573G= , CM000674.1:g.52841573G=	GRCh37
NC_000012.10:g.51127840G=	NCBI36
NG_008299.1:g.9338C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252252.4:c.1413C= MANE Select	ENSP00000252252.3:p.Gly471=
ENST00000252252.3:c.1413C=	ENSP00000252252.3:p.Gly471=
NM_005555.3:c.1413C=	NP_005546.2:p.Gly471=
NM_005555.4:c.1413C= MANE Select	NP_005546.2:p.Gly471=