Canonical Allele Identifier: CA1222574962
Gene: HLX-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.220836661A= , CM000663.2:g.220836661A= GRCh38
NC_000001.10:g.221010003A= , CM000663.1:g.221010003A= GRCh37
NC_000001.9:g.219076626A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651706.1:c.842+31387A= ENSP00000499157.1:n.842+31387A=
NR_046901.1:n.293-3469T=