Canonical Allele Identifier: CA448285668
Gene: LINC03066 HGNC NCBI
MyVariant.info:
GRCh38 chr6:g.204909G>A
GRCh37 chr6:g.204909G>A
gnomAD v3:
6:204909 G / A
gnomAD v4:
chr6-204909-G-A
Joint Max Group AF 0.00000488 (NFE)
Genomes Max Group AF 0.00000488 (NFE)
dbSNP:
7762550
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NR_126020.1:n.576C>T
Search 100 bp 5'
Search 100 bp 3'