Canonical Allele Identifier: CA672207786
Gene: APOA1-AS HGNC NCBI

Linked Data

dbSNP Id: rs1411911591
MyVariant Identifiers: chr11:g.116710917A>G (hg19) chr11:g.116840201A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116840201A>G , CM000673.2:g.116840201A>G GRCh38
NC_000011.9:g.116710917A>G , CM000673.1:g.116710917A>G GRCh37
NC_000011.8:g.116216127A>G NCBI36
NG_012021.1:g.2422T>C , LRG_767:g.2422T>C

Transcript Alleles

HGVS Amino-acid Change
NR_126362.1:n.123+3962A>G
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