Canonical Allele Identifier: CA1403171862

Gene: RAB6B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133839317C= , CM000665.2:g.133839317C=	GRCh38
NC_000003.11:g.133558161C= , CM000665.1:g.133558161C=	GRCh37
NC_000003.10:g.135040851C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000285208.9:c.401+189G= MANE Select	ENSP00000285208.4:n.401+189G=
ENST00000285208.8:c.401+189G=	ENSP00000285208.4:n.401+189G=
ENST00000460865.3:c.239+189G=	ENSP00000419526.3:n.239+189G=
ENST00000469959.1:c.96-11332G=	ENSP00000418540.1:n.96-11332G=
ENST00000477759.5:c.302+189G=	ENSP00000419941.1:n.302+189G=
ENST00000486858.5:c.362+189G=	ENSP00000419381.1:n.362+189G=
ENST00000543906.5:c.401+189G=	ENSP00000437797.1:n.401+189G=
NM_016577.3:c.401+189G=	NP_057661.3:n.401+189G=
XM_011512893.1:c.362+189G=	XP_011511195.1:n.362+189G=
NM_001363953.1:c.362+189G=	NP_001350882.1:n.362+189G=
NM_016577.4:c.401+189G= MANE Select	NP_057661.3:n.401+189G=