Canonical Allele Identifier: CA1012539649
Gene: HLX-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1048081686
gnomAD v3: 1-220837269-T-A
gnomAD v4: 1-220837269-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.220837269T>A , CM000663.2:g.220837269T>A GRCh38
NC_000001.10:g.221010611T>A , CM000663.1:g.221010611T>A GRCh37
NC_000001.9:g.219077234T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651706.1:c.842+31995T>A ENSP00000499157.1:n.842+31995T>A
NR_046901.1:n.293-4077A>T
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