Canonical Allele Identifier: CA37612924

Gene: HLX-AS1

Linked Data

• dbSNP Id: rs892370794
• gnomAD v2: 1-221010203-A-G
• gnomAD v3: 1-220836861-A-G
• gnomAD v4: 1-220836861-A-G
• MyVariant Identifiers: chr1:g.221010203A>G (hg19) ; chr1:g.220836861A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.220836861A>G , CM000663.2:g.220836861A>G	GRCh38
NC_000001.10:g.221010203A>G , CM000663.1:g.221010203A>G	GRCh37
NC_000001.9:g.219076826A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651706.1:c.842+31587A>G	ENSP00000499157.1:n.842+31587A>G
NR_046901.1:n.293-3669T>C