Canonical Allele Identifier: CA1138608137
Gene: RAB39B HGNC NCBI

Linked Data

dbSNP Id: rs2074845855
gnomAD v3: X-155259664-A-G
gnomAD v4: X-155259664-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.155259664A>G , CM000685.2:g.155259664A>G GRCh38
NC_000023.10:g.154488949A>G , CM000685.1:g.154488949A>G GRCh37
NC_000023.9:g.154142143A>G NCBI36
NG_012626.2:g.9898T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369454.4:c.*1139T>C MANE Select ENSP00000358466.3:n.*1139T>C
ENST00000369454.3:c.*1139T>C ENSP00000358466.3:n.*1139T>C
NM_171998.3:c.*1139T>C NP_741995.1:n.*1139T>C
NM_171998.4:c.*1139T>C MANE Select NP_741995.1:n.*1139T>C
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