Canonical Allele Identifier: CA37626447
Gene: HLX-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs11118620

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.220855166T>C , CM000663.2:g.220855166T>C GRCh38
NC_000001.10:g.221028508T>C , CM000663.1:g.221028508T>C GRCh37
NC_000001.9:g.219095131T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000651706.1:c.843-26028T>C ENSP00000499157.1:n.843-26028T>C
NR_046901.1:n.293-21974A>G