Canonical Allele Identifier: CA134433506
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs977535218
gnomAD v2: 6-6588692-A-G
gnomAD v3: 6-6588459-A-G
gnomAD v4: 6-6588459-A-G
MyVariant Identifiers: chr6:g.6588692A>G (hg19) chr6:g.6588459A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588459A>G , CM000668.2:g.6588459A>G GRCh38
NC_000006.11:g.6588692A>G , CM000668.1:g.6588692A>G GRCh37
NC_000006.10:g.6533691A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000379953.6:c.-10+9A>G (LY86) ENSP00000369286.1:n.-10+9A>G
NR_026970.1:n.196-18970T>C (LY86-AS1)
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