Canonical Allele Identifier: CA225853759
Gene: RAB38 HGNC NCBI

Linked Data

dbSNP Id: rs920073209
MyVariant Identifiers: chr11:g.87819381C>T (hg19) chr11:g.88086213C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.88086213C>T , CM000673.2:g.88086213C>T GRCh38
NC_000011.9:g.87819381C>T , CM000673.1:g.87819381C>T GRCh37
NC_000011.8:g.87459029C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017017455.2:c.483+63462G>A XP_016872944.1:n.483+63462G>A
XM_017017456.2:c.483+63462G>A XP_016872945.1:n.483+63462G>A
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