Canonical Allele Identifier: CA645253752
Gene: RAB39B HGNC NCBI

Linked Data

dbSNP Id: rs1483245211
gnomAD v2: X-154489088-GCT-G
gnomAD v3: X-155259803-GCT-G
gnomAD v4: X-155259803-GCT-G
MyVariant Identifiers: chrX:g.154489089_154489090del (hg19) chrX:g.155259804_155259805del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.155259806_155259807del , CM000685.2:g.155259806_155259807del GRCh38
NC_000023.10:g.154489091_154489092del , CM000685.1:g.154489091_154489092del GRCh37
NC_000023.9:g.154142285_154142286del NCBI36
NG_012626.2:g.9757_9758del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369454.4:c.*998_*999del MANE Select ENSP00000358466.3:n.*998_*999del
ENST00000369454.3:c.*998_*999del ENSP00000358466.3:n.*998_*999del
NM_171998.3:c.*998_*999del NP_741995.1:n.*998_*999del
NM_171998.4:c.*998_*999del MANE Select NP_741995.1:n.*998_*999del
Search 100 bp 5'
Search 100 bp 3'