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