Canonical Allele Identifier: CA827168684

Gene: LY86 LY86-AS1

Linked Data

• dbSNP Id: rs1407480620
• gnomAD v3: 6-6610195-C-T
• gnomAD v4: 6-6610195-C-T
• MyVariant Identifiers: chr6:g.6610428C>T (hg19) ; chr6:g.6610195C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6610195C>T , CM000668.2:g.6610195C>T	GRCh38
NC_000006.11:g.6610428C>T , CM000668.1:g.6610428C>T	GRCh37
NC_000006.10:g.6555427C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230568.5:c.137-14731C>T (LY86) MANE Select	ENSP00000230568.3:n.137-14731C>T
ENST00000230568.4:c.137-14731C>T (LY86)	ENSP00000230568.3:n.137-14731C>T
ENST00000379953.6:c.137-14731C>T (LY86)	ENSP00000369286.1:n.137-14731C>T
NM_004271.3:c.137-14731C>T (LY86)	NP_004262.1:n.137-14731C>T
NR_026970.1:n.195+12437G>A (LY86-AS1)
XM_017011505.1:c.137-14731C>T (LY86)	XP_016866994.1:n.137-14731C>T
NM_004271.4:c.137-14731C>T (LY86) MANE Select	NP_004262.1:n.137-14731C>T