Canonical Allele Identifier: CA2698210573
Gene: HLX-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs2102624638

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.220836877C>T , CM000663.2:g.220836877C>T GRCh38
NC_000001.10:g.221010219C>T , CM000663.1:g.221010219C>T GRCh37
NC_000001.9:g.219076842C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000651706.1:c.842+31603C>T ENSP00000499157.1:n.842+31603C>T
NR_046901.1:n.293-3685G>A