Canonical Allele Identifier: CA565308538
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1421260766
gnomAD v2: 6-6588889-T-C
gnomAD v3: 6-6588656-T-C
gnomAD v4: 6-6588656-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588656T>C , CM000668.2:g.6588656T>C GRCh38
NC_000006.11:g.6588889T>C , CM000668.1:g.6588889T>C GRCh37
NC_000006.10:g.6533888T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000379953.6:c.-9-70T>C (LY86) ENSP00000369286.1:n.-9-70T>C
NR_026970.1:n.196-19167A>G (LY86-AS1)
XM_017011505.1:c.-79T>C (LY86) XP_016866994.1:n.-79T>C