Canonical Allele Identifier: CA1989382903
Gene: RAB38 HGNC NCBI

Linked Data

dbSNP Id: rs1942131980

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.88086183T>C , CM000673.2:g.88086183T>C GRCh38
NC_000011.9:g.87819351T>C , CM000673.1:g.87819351T>C GRCh37
NC_000011.8:g.87458999T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017017455.2:c.483+63492A>G XP_016872944.1:n.483+63492A>G
XM_017017456.2:c.483+63492A>G XP_016872945.1:n.483+63492A>G