Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48045781C= , CM000675.2:g.48045781C= | GRCh38 |
| NC_000013.10:g.48619917C= , CM000675.1:g.48619917C= | GRCh37 |
| NC_000013.9:g.47517918C= | NCBI36 |
| NG_047021.1:g.13215C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258662.3:c.477C= MANE Select | ENSP00000258662.1:p.Tyr159= | |
| ENST00000258662.2:c.477C= | ENSP00000258662.1:p.Tyr159= | |
| NM_018283.2:c.477C= | NP_060753.1:p.Tyr159= | |
| NM_018283.3:c.477C= | NP_060753.1:p.Tyr159= | |
| NR_136687.1:n.657C= | ||
| NR_136688.1:n.657C= | ||
| NM_018283.4:c.477C= MANE Select | NP_060753.1:p.Tyr159= | |
| NR_136687.2:n.498C= | ||
| NR_136688.2:n.498C= |