Canonical Allele Identifier: CA2695179890
Gene: RAB39B HGNC NCBI

Linked Data

gnomAD v4: X-155259833-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.155259833C>A , CM000685.2:g.155259833C>A GRCh38
NC_000023.10:g.154489118C>A , CM000685.1:g.154489118C>A GRCh37
NC_000023.9:g.154142312C>A NCBI36
NG_012626.2:g.9729G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369454.4:c.*970G>T MANE Select ENSP00000358466.3:n.*970G>T
ENST00000369454.3:c.*970G>T ENSP00000358466.3:n.*970G>T
NM_171998.3:c.*970G>T NP_741995.1:n.*970G>T
NM_171998.4:c.*970G>T MANE Select NP_741995.1:n.*970G>T
Search 100 bp 5'
Search 100 bp 3'