Canonical Allele Identifier: CA12670668
Gene: LINC02889 HGNC NCBI
COSMIC:
COSN20481379 (not active)
MyVariant.info:
GRCh38 chr7:g.17521959A>G
GRCh37 chr7:g.17561583A>G
gnomAD v2:
7:17561583 A / G
gnomAD v3:
7:17521959 A / G
gnomAD v4:
chr7-17521959-A-G
Joint Max Group AF 0.21517172 (SAS)
Genomes Max Group AF 0.21517172 (SAS)
dbSNP:
10499504
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17521959A>G , CM000669.2:g.17521959A>G GRCh38
NC_000007.13:g.17561583A>G , CM000669.1:g.17561583A>G GRCh37
NC_000007.12:g.17528108A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110013.1:n.158+36793T>C
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