Canonical Allele Identifier: CA986287846
Gene: RAB37 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.74670881G>T , CM000679.2:g.74670881G>T GRCh38
NC_000017.10:g.72667020G>T , CM000679.1:g.72667020G>T GRCh37
NC_000017.9:g.70178615G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000340415.7:c.-706G>T ENSP00000341354.3:n.-706G>T
XR_001753013.2:n.5739C>A