Canonical Allele Identifier: CA672207778
Gene: APOA1-AS HGNC NCBI

Linked Data

dbSNP Id: rs1171419868
MyVariant Identifiers: chr11:g.116710908G>A (hg19) chr11:g.116840192G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116840192G>A , CM000673.2:g.116840192G>A GRCh38
NC_000011.9:g.116710908G>A , CM000673.1:g.116710908G>A GRCh37
NC_000011.8:g.116216118G>A NCBI36
NG_012021.1:g.2431C>T , LRG_767:g.2431C>T

Transcript Alleles

HGVS Amino-acid Change
NR_126362.1:n.123+3953G>A
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