Canonical Allele Identifier: CA731823952
Gene: HLX-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1369724851
MyVariant Identifiers: chr1:g.221009999G>A (hg19) chr1:g.220836657G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.220836657G>A , CM000663.2:g.220836657G>A GRCh38
NC_000001.10:g.221009999G>A , CM000663.1:g.221009999G>A GRCh37
NC_000001.9:g.219076622G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651706.1:c.842+31383G>A ENSP00000499157.1:n.842+31383G>A
NR_046901.1:n.293-3465C>T
Search 100 bp 5'
Search 100 bp 3'