Canonical Allele Identifier: CA134433507
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs2233118
gnomAD v2: 6-6588693-C-T
gnomAD v3: 6-6588460-C-T
gnomAD v4: 6-6588460-C-T
MyVariant Identifiers: chr6:g.6588693C>T (hg19) chr6:g.6588460C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588460C>T , CM000668.2:g.6588460C>T GRCh38
NC_000006.11:g.6588693C>T , CM000668.1:g.6588693C>T GRCh37
NC_000006.10:g.6533692C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000379953.6:c.-10+10C>T (LY86) ENSP00000369286.1:n.-10+10C>T
NR_026970.1:n.196-18971G>A (LY86-AS1)
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