Canonical Allele Identifier: CA37613227

Gene: HLX-AS1

Linked Data

• dbSNP Id: rs934767325
• MyVariant Identifiers: chr1:g.221010477A>G (hg19) ; chr1:g.220837135A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.220837135A>G , CM000663.2:g.220837135A>G	GRCh38
NC_000001.10:g.221010477A>G , CM000663.1:g.221010477A>G	GRCh37
NC_000001.9:g.219077100A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651706.1:c.842+31861A>G	ENSP00000499157.1:n.842+31861A>G
NR_046901.1:n.293-3943T>C