Canonical Allele Identifier: CA1403180089
Community Standard Title: NM_016577.4(RAB6B):c.71-5838G=
Gene: RAB6B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.133870480C= , CM000665.2:g.133870480C= GRCh38
NC_000003.11:g.133589324C= , CM000665.1:g.133589324C= GRCh37
NC_000003.10:g.135072014C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_016577.4:c.71-5838G= MANE Select NP_057661.3:n.71-5838G=
ENST00000285208.9:c.71-5838G= MANE Select ENSP00000285208.4:n.71-5838G=
NM_001363953.1:c.32-5838G= NP_001350882.1:n.32-5838G=
NM_016577.3:c.71-5838G= NP_057661.3:n.71-5838G=
ENST00000285208.8:c.71-5838G= ENSP00000285208.4:n.71-5838G=
ENST00000460865.3:c.-34+24917G= ENSP00000419526.3:n.-34+24917G=
ENST00000469959.1:c.71-5838G= ENSP00000418540.1:n.71-5838G=
ENST00000477759.5:c.-29-5838G= ENSP00000419941.1:n.-29-5838G=
ENST00000486858.5:c.32-5838G= ENSP00000419381.1:n.32-5838G=
ENST00000488969.1:c.-29-5838G= ENSP00000417433.1:n.-29-5838G=
ENST00000543906.5:c.71-5838G= ENSP00000437797.1:n.71-5838G=
XM_011512893.1:c.32-5838G= XP_011511195.1:n.32-5838G=