Canonical Allele Identifier: CA2466944628
Gene: RAB39B HGNC NCBI

Linked Data

dbSNP Id: rs1602911880
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.155259842C>T , CM000685.2:g.155259842C>T GRCh38
NC_000023.10:g.154489127C>T , CM000685.1:g.154489127C>T GRCh37
NC_000023.9:g.154142321C>T NCBI36
NG_012626.2:g.9720G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369454.4:c.*961G>A MANE Select ENSP00000358466.3:n.*961G>A
ENST00000369454.3:c.*961G>A ENSP00000358466.3:n.*961G>A
NM_171998.3:c.*961G>A NP_741995.1:n.*961G>A
NM_171998.4:c.*961G>A MANE Select NP_741995.1:n.*961G>A
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