Canonical Allele Identifier: CA1989382930
Gene: RAB38 HGNC NCBI

Linked Data

dbSNP Id: rs1942132220
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.88086209G>T , CM000673.2:g.88086209G>T GRCh38
NC_000011.9:g.87819377G>T , CM000673.1:g.87819377G>T GRCh37
NC_000011.8:g.87459025G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017017455.2:c.483+63466C>A XP_016872944.1:n.483+63466C>A
XM_017017456.2:c.483+63466C>A XP_016872945.1:n.483+63466C>A
Search 100 bp 5'
Search 100 bp 3'