Canonical Allele Identifier: CA134432891
Gene: LY86-AS1 HGNC NCBI
COSMIC:
COSN20464803 (not active)
MyVariant.info:
GRCh38 chr6:g.6583488G>A
GRCh37 chr6:g.6583721G>A
gnomAD v2:
6:6583721 G / A
gnomAD v3:
6:6583488 G / A
gnomAD v4:
chr6-6583488-G-A
Joint Max Group AF 0.91064564 (EAS)
Genomes Max Group AF 0.91064564 (EAS)
dbSNP:
1334710
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6583488G>A , CM000668.2:g.6583488G>A GRCh38
NC_000006.11:g.6583721G>A , CM000668.1:g.6583721G>A GRCh37
NC_000006.10:g.6528720G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_026970.1:n.196-13999C>T
Search 100 bp 5'
Search 100 bp 3'