Canonical Allele Identifier: CA59129062
Gene: LINC01876 HGNC NCBI
dbSNP:
10177924
gnomAD v2:
2:156933553 A / G
gnomAD v3:
2:156077041 A / G
gnomAD v4:
chr2-156077041-A-G
Joint Max Group AF 0.3047069 (SAS)
Genomes Max Group AF 0.3047069 (SAS)
MyVariant.info:
GRCh38 chr2:g.156077041A>G
GRCh37 chr2:g.156933553A>G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.156077041A>G , CM000664.2:g.156077041A>G GRCh38
NC_000002.11:g.156933553A>G , CM000664.1:g.156933553A>G GRCh37
NC_000002.10:g.156641799A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110249.2:n.155-52465T>C
NR_110250.2:n.155-52434T>C
Search 100 bp 5'
Search 100 bp 3'