Canonical Allele Identifier: CA827168722

Gene: LY86 LY86-AS1

Linked Data

• dbSNP Id: rs1365454198
• gnomAD v3: 6-6610252-G-A
• gnomAD v4: 6-6610252-G-A
• MyVariant Identifiers: chr6:g.6610485G>A (hg19) ; chr6:g.6610252G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6610252G>A , CM000668.2:g.6610252G>A	GRCh38
NC_000006.11:g.6610485G>A , CM000668.1:g.6610485G>A	GRCh37
NC_000006.10:g.6555484G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230568.5:c.137-14674G>A (LY86) MANE Select	ENSP00000230568.3:n.137-14674G>A
ENST00000230568.4:c.137-14674G>A (LY86)	ENSP00000230568.3:n.137-14674G>A
ENST00000379953.6:c.137-14674G>A (LY86)	ENSP00000369286.1:n.137-14674G>A
NM_004271.3:c.137-14674G>A (LY86)	NP_004262.1:n.137-14674G>A
NR_026970.1:n.195+12380C>T (LY86-AS1)
XM_017011505.1:c.137-14674G>A (LY86)	XP_016866994.1:n.137-14674G>A
NM_004271.4:c.137-14674G>A (LY86) MANE Select	NP_004262.1:n.137-14674G>A