Canonical Allele Identifier: CA1989382912
Gene: RAB38 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.88086201A= , CM000673.2:g.88086201A= GRCh38
NC_000011.9:g.87819369A= , CM000673.1:g.87819369A= GRCh37
NC_000011.8:g.87459017A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017017455.2:c.483+63474T= XP_016872944.1:n.483+63474T=
XM_017017456.2:c.483+63474T= XP_016872945.1:n.483+63474T=