Canonical Allele Identifier: CA1989383023
Gene: RAB38 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.88086259T= , CM000673.2:g.88086259T= GRCh38
NC_000011.9:g.87819427T= , CM000673.1:g.87819427T= GRCh37
NC_000011.8:g.87459075T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017017455.2:c.483+63416A= XP_016872944.1:n.483+63416A=
XM_017017456.2:c.483+63416A= XP_016872945.1:n.483+63416A=