Canonical Allele Identifier: CA827150022
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1471171053

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588565T>C , CM000668.2:g.6588565T>C GRCh38
NC_000006.11:g.6588798T>C , CM000668.1:g.6588798T>C GRCh37
NC_000006.10:g.6533797T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000379953.6:c.-10+115T>C (LY86) ENSP00000369286.1:n.-10+115T>C
NR_026970.1:n.196-19076A>G (LY86-AS1)