Canonical Allele Identifier: CA12239056
Gene: LINC02549 HGNC NCBI
dbSNP:
10455657
gnomAD v2:
6:68984930 T / G
gnomAD v3:
6:68275038 T / G
gnomAD v4:
chr6-68275038-T-G
Joint Max Group AF 0.37852182 (AFR)
Genomes Max Group AF 0.37852182 (AFR)
MyVariant.info:
GRCh38 chr6:g.68275038T>G
GRCh37 chr6:g.68984930T>G
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.68275038T>G , CM000668.2:g.68275038T>G GRCh38
NC_000006.11:g.68984930T>G , CM000668.1:g.68984930T>G GRCh37
NC_000006.10:g.69041651T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125854.1:n.238-8423A>C
Search 100 bp 5'
Search 100 bp 3'