Canonical Allele Identifier: CA12223198
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI
MyVariant.info:
GRCh38 chr6:g.6588648A>C
GRCh37 chr6:g.6588881A>C
gnomAD v2:
6:6588881 A / C
gnomAD v3:
6:6588648 A / C
gnomAD v4:
chr6-6588648-A-C
Joint Max Group AF 0.75016346 (MID)
Genomes Max Group AF 0.72944074 (NFE)
Exomes Max Group AF 0.75170231 (MID)
dbSNP:
977785
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588648A>C , CM000668.2:g.6588648A>C GRCh38
NC_000006.11:g.6588881A>C , CM000668.1:g.6588881A>C GRCh37
NC_000006.10:g.6533880A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000379953.6:c.-9-78A>C (LY86) ENSP00000369286.1:n.-9-78A>C
NR_026970.1:n.196-19159T>G (LY86-AS1)
XM_017011505.1:c.-87A>C (LY86) XP_016866994.1:n.-87A>C
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