Canonical Allele Identifier: CA2677195569
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

gnomAD v4: 6-6588567-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588567C>A , CM000668.2:g.6588567C>A GRCh38
NC_000006.11:g.6588800C>A , CM000668.1:g.6588800C>A GRCh37
NC_000006.10:g.6533799C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000379953.6:c.-10+117C>A (LY86) ENSP00000369286.1:n.-10+117C>A
NR_026970.1:n.196-19078G>T (LY86-AS1)