Canonical Allele Identifier: CA1403171875

Gene: RAB6B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133839346T= , CM000665.2:g.133839346T=	GRCh38
NC_000003.11:g.133558190T= , CM000665.1:g.133558190T=	GRCh37
NC_000003.10:g.135040880T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000285208.9:c.401+160A= MANE Select	ENSP00000285208.4:n.401+160A=
ENST00000285208.8:c.401+160A=	ENSP00000285208.4:n.401+160A=
ENST00000460865.3:c.239+160A=	ENSP00000419526.3:n.239+160A=
ENST00000469959.1:c.96-11361A=	ENSP00000418540.1:n.96-11361A=
ENST00000477759.5:c.302+160A=	ENSP00000419941.1:n.302+160A=
ENST00000486858.5:c.362+160A=	ENSP00000419381.1:n.362+160A=
ENST00000543906.5:c.401+160A=	ENSP00000437797.1:n.401+160A=
NM_016577.3:c.401+160A=	NP_057661.3:n.401+160A=
XM_011512893.1:c.362+160A=	XP_011511195.1:n.362+160A=
NM_001363953.1:c.362+160A=	NP_001350882.1:n.362+160A=
NM_016577.4:c.401+160A= MANE Select	NP_057661.3:n.401+160A=