Canonical Allele Identifier: CA37613340
Gene: HLX-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1048081686
MyVariant Identifiers: chr1:g.221010611T>G (hg19) chr1:g.220837269T>G (hg38)
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Genomic Alleles

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

Transcript Alleles

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