Canonical Allele Identifier: CA1222592058
Gene: HLX-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1674354553

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.220878437dup , CM000663.2:g.220878437dup GRCh38
NC_000001.10:g.221051779dup , CM000663.1:g.221051779dup GRCh37
NC_000001.9:g.219118402dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651706.1:c.843-2757dup ENSP00000499157.1:n.843-2757dup
NR_046901.1:n.292+1413dup
XM_011510307.1:c.623dup XP_011508609.1:p.Gly209TrpfsTer12