Canonical Allele Identifier: CA225853751
Gene: RAB38 HGNC NCBI

Linked Data

dbSNP Id: rs914319778
gnomAD v3: 11-88086164-T-C
gnomAD v4: 11-88086164-T-C
MyVariant Identifiers: chr11:g.87819332T>C (hg19) chr11:g.88086164T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.88086164T>C , CM000673.2:g.88086164T>C GRCh38
NC_000011.9:g.87819332T>C , CM000673.1:g.87819332T>C GRCh37
NC_000011.8:g.87458980T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017017455.2:c.483+63511A>G XP_016872944.1:n.483+63511A>G
XM_017017456.2:c.483+63511A>G XP_016872945.1:n.483+63511A>G
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