Canonical Allele Identifier: CA2531335786
Gene: RAB39B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.155259770del , CM000685.2:g.155259770del GRCh38
NC_000023.10:g.154489055del , CM000685.1:g.154489055del GRCh37
NC_000023.9:g.154142249del NCBI36
NG_012626.2:g.9792del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369454.4:c.*1033del MANE Select ENSP00000358466.3:n.*1033del
ENST00000369454.3:c.*1033del ENSP00000358466.3:n.*1033del
NM_171998.3:c.*1033del NP_741995.1:n.*1033del
NM_171998.4:c.*1033del MANE Select NP_741995.1:n.*1033del
Search 100 bp 5'
Search 100 bp 3'