Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.6610155G>C , CM000668.2:g.6610155G>C | GRCh38 |
| NC_000006.11:g.6610388G>C , CM000668.1:g.6610388G>C | GRCh37 |
| NC_000006.10:g.6555387G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000230568.5:c.137-14771G>C (LY86) MANE Select | ENSP00000230568.3:n.137-14771G>C | |
| ENST00000230568.4:c.137-14771G>C (LY86) | ENSP00000230568.3:n.137-14771G>C | |
| ENST00000379953.6:c.137-14771G>C (LY86) | ENSP00000369286.1:n.137-14771G>C | |
| NM_004271.3:c.137-14771G>C (LY86) | NP_004262.1:n.137-14771G>C | |
| NR_026970.1:n.195+12477C>G (LY86-AS1) | ||
| XM_017011505.1:c.137-14771G>C (LY86) | XP_016866994.1:n.137-14771G>C | |
| NM_004271.4:c.137-14771G>C (LY86) MANE Select | NP_004262.1:n.137-14771G>C |