Canonical Allele Identifier: CA83687394

Gene: RAB6B

Linked Data

• dbSNP Id: rs938143493
• gnomAD v3: 3-133839318-A-G
• gnomAD v4: 3-133839318-A-G
• MyVariant Identifiers: chr3:g.133558162A>G (hg19) ; chr3:g.133839318A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133839318A>G , CM000665.2:g.133839318A>G	GRCh38
NC_000003.11:g.133558162A>G , CM000665.1:g.133558162A>G	GRCh37
NC_000003.10:g.135040852A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285208.9:c.401+188T>C MANE Select	ENSP00000285208.4:n.401+188T>C
ENST00000285208.8:c.401+188T>C	ENSP00000285208.4:n.401+188T>C
ENST00000460865.3:c.239+188T>C	ENSP00000419526.3:n.239+188T>C
ENST00000469959.1:c.96-11333T>C	ENSP00000418540.1:n.96-11333T>C
ENST00000477759.5:c.302+188T>C	ENSP00000419941.1:n.302+188T>C
ENST00000486858.5:c.362+188T>C	ENSP00000419381.1:n.362+188T>C
ENST00000543906.5:c.401+188T>C	ENSP00000437797.1:n.401+188T>C
NM_016577.3:c.401+188T>C	NP_057661.3:n.401+188T>C
XM_011512893.1:c.362+188T>C	XP_011511195.1:n.362+188T>C
NM_001363953.1:c.362+188T>C	NP_001350882.1:n.362+188T>C
NM_016577.4:c.401+188T>C MANE Select	NP_057661.3:n.401+188T>C