Canonical Allele Identifier: CA823831599
Gene: LINC00243 HGNC NCBI
MyVariant.info:
GRCh38 chr6:g.30821870G>A
GRCh37 chr6:g.30789647G>A
gnomAD v3:
6:30821870 G / A
gnomAD v4:
chr6-30821870-G-A
Joint Max Group AF 0.00021529 (AMR)
Genomes Max Group AF 0.00021529 (AMR)
dbSNP:
1264352
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30821870G>A , CM000668.2:g.30821870G>A GRCh38
NC_000006.11:g.30789647G>A , CM000668.1:g.30789647G>A GRCh37
NC_000006.10:g.30897626G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130726.1:n.146-7098C>T
Search 100 bp 5'
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