Canonical Allele Identifier: CA731823942

Gene: HLX-AS1

Linked Data

• dbSNP Id: rs1312610362
• gnomAD v3: 1-220836627-A-T
• gnomAD v4: 1-220836627-A-T
• MyVariant Identifiers: chr1:g.221009969A>T (hg19) ; chr1:g.220836627A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.220836627A>T , CM000663.2:g.220836627A>T	GRCh38
NC_000001.10:g.221009969A>T , CM000663.1:g.221009969A>T	GRCh37
NC_000001.9:g.219076592A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651706.1:c.842+31353A>T	ENSP00000499157.1:n.842+31353A>T
NR_046901.1:n.293-3435T>A