Canonical Allele Identifier: CA2677195505
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

gnomAD v4: 6-6588500-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588500A>T , CM000668.2:g.6588500A>T GRCh38
NC_000006.11:g.6588733A>T , CM000668.1:g.6588733A>T GRCh37
NC_000006.10:g.6533732A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000379953.6:c.-10+50A>T (LY86) ENSP00000369286.1:n.-10+50A>T
NR_026970.1:n.196-19011T>A (LY86-AS1)