dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.6588648A>T , CM000668.2:g.6588648A>T | GRCh38 |
| NC_000006.11:g.6588881A>T , CM000668.1:g.6588881A>T | GRCh37 |
| NC_000006.10:g.6533880A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000379953.6:c.-9-78A>T (LY86) | ENSP00000369286.1:n.-9-78A>T | |
| NR_026970.1:n.196-19159T>A (LY86-AS1) | ||
| XM_017011505.1:c.-87A>T (LY86) | XP_016866994.1:n.-87A>T |