Canonical Allele Identifier: CA15474084
Gene: LINC03066 HGNC NCBI
MyVariant.info:
GRCh38 chr6:g.204909G>T
GRCh37 chr6:g.204909G>T
gnomAD v2:
6:204909 G / T
gnomAD v3:
6:204909 G / T
gnomAD v4:
chr6-204909-G-T
Joint Max Group AF 0.71211319 (AFR)
Genomes Max Group AF 0.71212338 (AFR)
Exomes Max Group AF 0.13209035 (NFE)
dbSNP:
7762550
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.204909G>T , CM000668.2:g.204909G>T GRCh38
NC_000006.11:g.204909G>T , CM000668.1:g.204909G>T GRCh37
NC_000006.10:g.149909G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126020.1:n.576C>A
Search 100 bp 5'
Search 100 bp 3'