Canonical Allele Identifier: CA731824175
Gene: HLX-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1411578781
MyVariant Identifiers: chr1:g.221010614G>C (hg19) chr1:g.220837272G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.220837272G>C , CM000663.2:g.220837272G>C GRCh38
NC_000001.10:g.221010614G>C , CM000663.1:g.221010614G>C GRCh37
NC_000001.9:g.219077237G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651706.1:c.842+31998G>C ENSP00000499157.1:n.842+31998G>C
NR_046901.1:n.293-4080C>G
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