Canonical Allele Identifier: CA2321403956
Gene: RAB11B HGNC NCBI
ELAVL1 HGNC NCBI

Linked Data

dbSNP Id: rs1971464692

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8404415T>C , CM000681.2:g.8404415T>C GRCh38
NC_000019.9:g.8469299T>C , CM000681.1:g.8469299T>C GRCh37
NC_000019.8:g.8375299T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000328024.11:c.*857T>C (RAB11B) MANE Select ENSP00000333547.5:n.*857T>C
ENST00000328024.10:c.*857T>C (RAB11B) ENSP00000333547.5:n.*857T>C
ENST00000351593.9:c.-88+40591A>G (ELAVL1) ENSP00000264073.6:n.-88+40591A>G
NM_004218.3:c.*857T>C (RAB11B) NP_004209.2:n.*857T>C
NM_004218.4:c.*857T>C (RAB11B) MANE Select NP_004209.2:n.*857T>C