Canonical Allele Identifier: CA12179189
Gene: LY86-AS1 HGNC NCBI
MyVariant.info:
GRCh38 chr6:g.6547254C>A
GRCh37 chr6:g.6547487C>A
gnomAD v2:
6:6547487 C / A
gnomAD v3:
6:6547254 C / A
gnomAD v4:
chr6-6547254-C-A
Joint Max Group AF 0.5263999 (MID)
Genomes Max Group AF 0.45624121 (NFE)
dbSNP:
554653
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6547254C>A , CM000668.2:g.6547254C>A GRCh38
NC_000006.11:g.6547487C>A , CM000668.1:g.6547487C>A GRCh37
NC_000006.10:g.6492486C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_026970.1:n.361+17041G>T
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