Canonical Allele Identifier: CA529064251
Gene: HLX-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1210550627

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.220836626T>C , CM000663.2:g.220836626T>C GRCh38
NC_000001.10:g.221009968T>C , CM000663.1:g.221009968T>C GRCh37
NC_000001.9:g.219076591T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651706.1:c.842+31352T>C ENSP00000499157.1:n.842+31352T>C
NR_046901.1:n.293-3434A>G