Canonical Allele Identifier: CA2466944636
Gene: RAB39B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.155259857A= , CM000685.2:g.155259857A= GRCh38
NC_000023.10:g.154489142A= , CM000685.1:g.154489142A= GRCh37
NC_000023.9:g.154142336A= NCBI36
NG_012626.2:g.9705T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369454.4:c.*946T= MANE Select ENSP00000358466.3:n.*946T=
ENST00000369454.3:c.*946T= ENSP00000358466.3:n.*946T=
NM_171998.3:c.*946T= NP_741995.1:n.*946T=
NM_171998.4:c.*946T= MANE Select NP_741995.1:n.*946T=
Search 100 bp 5'
Search 100 bp 3'