Canonical Allele Identifier: CA134433526

Gene: LY86 LY86-AS1

Linked Data

• dbSNP Id: rs2233119
• gnomAD v2: 6-6588805-G-A
• gnomAD v3: 6-6588572-G-A
• gnomAD v4: 6-6588572-G-A
• MyVariant Identifiers: chr6:g.6588805G>A (hg19) ; chr6:g.6588572G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6588572G>A , CM000668.2:g.6588572G>A	GRCh38
NC_000006.11:g.6588805G>A , CM000668.1:g.6588805G>A	GRCh37
NC_000006.10:g.6533804G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000379953.6:c.-10+122G>A (LY86)	ENSP00000369286.1:n.-10+122G>A
NR_026970.1:n.196-19083C>T (LY86-AS1)