Canonical Allele Identifier: CA134433509
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs944001923

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588463A>G , CM000668.2:g.6588463A>G GRCh38
NC_000006.11:g.6588696A>G , CM000668.1:g.6588696A>G GRCh37
NC_000006.10:g.6533695A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000379953.6:c.-10+13A>G (LY86) ENSP00000369286.1:n.-10+13A>G
NR_026970.1:n.196-18974T>C (LY86-AS1)