Canonical Allele Identifier: CA2466944613
Gene: RAB39B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.155259784T= , CM000685.2:g.155259784T= GRCh38
NC_000023.10:g.154489069T= , CM000685.1:g.154489069T= GRCh37
NC_000023.9:g.154142263T= NCBI36
NG_012626.2:g.9778A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369454.4:c.*1019A= MANE Select ENSP00000358466.3:n.*1019A=
ENST00000369454.3:c.*1019A= ENSP00000358466.3:n.*1019A=
NM_171998.3:c.*1019A= NP_741995.1:n.*1019A=
NM_171998.4:c.*1019A= MANE Select NP_741995.1:n.*1019A=
Search 100 bp 5'
Search 100 bp 3'