Canonical Allele Identifier: CA1222574959
Gene: HLX-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1369724851
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.220836657G>T , CM000663.2:g.220836657G>T GRCh38
NC_000001.10:g.221009999G>T , CM000663.1:g.221009999G>T GRCh37
NC_000001.9:g.219076622G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651706.1:c.842+31383G>T ENSP00000499157.1:n.842+31383G>T
NR_046901.1:n.293-3465C>A
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