Canonical Allele Identifier: CA2321403954
Gene: RAB11B HGNC NCBI
ELAVL1 HGNC NCBI

Linked Data

dbSNP Id: rs533242991

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8404414A>T , CM000681.2:g.8404414A>T GRCh38
NC_000019.9:g.8469298A>T , CM000681.1:g.8469298A>T GRCh37
NC_000019.8:g.8375298A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000328024.11:c.*856A>T (RAB11B) MANE Select ENSP00000333547.5:n.*856A>T
ENST00000328024.10:c.*856A>T (RAB11B) ENSP00000333547.5:n.*856A>T
ENST00000351593.9:c.-88+40592T>A (ELAVL1) ENSP00000264073.6:n.-88+40592T>A
NM_004218.3:c.*856A>T (RAB11B) NP_004209.2:n.*856A>T
NM_004218.4:c.*856A>T (RAB11B) MANE Select NP_004209.2:n.*856A>T