Canonical Allele Identifier: CA1222592074
Gene: HLX-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1674355328

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.220878466G>A , CM000663.2:g.220878466G>A GRCh38
NC_000001.10:g.221051808G>A , CM000663.1:g.221051808G>A GRCh37
NC_000001.9:g.219118431G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651706.1:c.843-2728G>A ENSP00000499157.1:n.843-2728G>A
NR_046901.1:n.292+1383C>T
XM_011510307.1:c.593C>T XP_011508609.1:p.Pro198Leu