Canonical Allele Identifier: CA1608139177
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1760420387

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588464T>C , CM000668.2:g.6588464T>C GRCh38
NC_000006.11:g.6588697T>C , CM000668.1:g.6588697T>C GRCh37
NC_000006.10:g.6533696T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000379953.6:c.-10+14T>C (LY86) ENSP00000369286.1:n.-10+14T>C
NR_026970.1:n.196-18975A>G (LY86-AS1)