Canonical Allele Identifier: CA1222592078
Gene: HLX-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1571710603

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.220878469G>T , CM000663.2:g.220878469G>T GRCh38
NC_000001.10:g.221051811G>T , CM000663.1:g.221051811G>T GRCh37
NC_000001.9:g.219118434G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651706.1:c.843-2725G>T ENSP00000499157.1:n.843-2725G>T
NR_046901.1:n.292+1380C>A
XM_011510307.1:c.590C>A XP_011508609.1:p.Thr197Asn