Canonical Allele Identifier: CA37613324
Gene: HLX-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs558149658
gnomAD v2: 1-221010600-A-C
gnomAD v3: 1-220837258-A-C
gnomAD v4: 1-220837258-A-C
MyVariant Identifiers: chr1:g.221010600A>C (hg19) chr1:g.220837258A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.220837258A>C , CM000663.2:g.220837258A>C GRCh38
NC_000001.10:g.221010600A>C , CM000663.1:g.221010600A>C GRCh37
NC_000001.9:g.219077223A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651706.1:c.842+31984A>C ENSP00000499157.1:n.842+31984A>C
NR_046901.1:n.293-4066T>G
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