Canonical Allele Identifier: CA2466944608
Gene: RAB39B HGNC NCBI

Linked Data

dbSNP Id: rs2074846168
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.155259767T>C , CM000685.2:g.155259767T>C GRCh38
NC_000023.10:g.154489052T>C , CM000685.1:g.154489052T>C GRCh37
NC_000023.9:g.154142246T>C NCBI36
NG_012626.2:g.9795A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369454.4:c.*1036A>G MANE Select ENSP00000358466.3:n.*1036A>G
ENST00000369454.3:c.*1036A>G ENSP00000358466.3:n.*1036A>G
NM_171998.3:c.*1036A>G NP_741995.1:n.*1036A>G
NM_171998.4:c.*1036A>G MANE Select NP_741995.1:n.*1036A>G
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