Canonical Allele Identifier: CA529064259
Gene: HLX-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1043132963
gnomAD v2: 1-221010187-C-A
gnomAD v3: 1-220836845-C-A
gnomAD v4: 1-220836845-C-A
MyVariant Identifiers: chr1:g.221010187C>A (hg19) chr1:g.220836845C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.220836845C>A , CM000663.2:g.220836845C>A GRCh38
NC_000001.10:g.221010187C>A , CM000663.1:g.221010187C>A GRCh37
NC_000001.9:g.219076810C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651706.1:c.842+31571C>A ENSP00000499157.1:n.842+31571C>A
NR_046901.1:n.293-3653G>T
Search 100 bp 5'
Search 100 bp 3'