Canonical Allele Identifier: CA1989382859
Gene: RAB38 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.88086160A= , CM000673.2:g.88086160A= GRCh38
NC_000011.9:g.87819328A= , CM000673.1:g.87819328A= GRCh37
NC_000011.8:g.87458976A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017017455.2:c.483+63515T= XP_016872944.1:n.483+63515T=
XM_017017456.2:c.483+63515T= XP_016872945.1:n.483+63515T=