Canonical Allele Identifier: CA14099796
Gene: C15orf48 HGNC NCBI
SLC30A4-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45448194G>A , CM000677.2:g.45448194G>A GRCh38
NC_000015.9:g.45740392G>A , CM000677.1:g.45740392G>A GRCh37
NC_000015.8:g.43527684G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000558435.5:c.184-355G>A (C15orf48) ENSP00000452967.1:n.184-355G>A
XM_017022774.1:c.166-124G>A (SLC30A4-AS1) XP_016878263.1:n.166-124G>A