Canonical Allele Identifier: CA899123578

Gene: RAB6B

Linked Data

• dbSNP Id: rs1164485222
• MyVariant Identifiers: chr3:g.133558194A>T (hg19) ; chr3:g.133839350A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133839350A>T , CM000665.2:g.133839350A>T	GRCh38
NC_000003.11:g.133558194A>T , CM000665.1:g.133558194A>T	GRCh37
NC_000003.10:g.135040884A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000285208.9:c.401+156T>A MANE Select	ENSP00000285208.4:n.401+156T>A
ENST00000285208.8:c.401+156T>A	ENSP00000285208.4:n.401+156T>A
ENST00000460865.3:c.239+156T>A	ENSP00000419526.3:n.239+156T>A
ENST00000469959.1:c.96-11365T>A	ENSP00000418540.1:n.96-11365T>A
ENST00000477759.5:c.302+156T>A	ENSP00000419941.1:n.302+156T>A
ENST00000486858.5:c.362+156T>A	ENSP00000419381.1:n.362+156T>A
ENST00000543906.5:c.401+156T>A	ENSP00000437797.1:n.401+156T>A
NM_016577.3:c.401+156T>A	NP_057661.3:n.401+156T>A
XM_011512893.1:c.362+156T>A	XP_011511195.1:n.362+156T>A
NM_001363953.1:c.362+156T>A	NP_001350882.1:n.362+156T>A
NM_016577.4:c.401+156T>A MANE Select	NP_057661.3:n.401+156T>A