Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.136659262C= , CM000685.2:g.136659262C= | GRCh38 |
| NC_000023.10:g.135741421C= , CM000685.1:g.135741421C= | GRCh37 |
| NC_000023.9:g.135569087C= | NCBI36 |
| NG_007280.1:g.16086C= , LRG_141:g.16086C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695724.1:c.*251C= | ENSP00000512122.1:n.*251C= | |
| ENST00000695725.1:c.*188C= | ENSP00000512123.1:n.*188C= | |
| ENST00000695726.1:n.2601C= | ||
| ENST00000695729.1:n.3436C= | ||
| ENST00000370629.7:c.633C= MANE Select | ENSP00000359663.2:p.Thr211= | |
| ENST00000370628.2:c.570C= | ENSP00000359662.2:p.Thr190= | |
| ENST00000370629.6:c.633C= | ENSP00000359663.2:p.Thr211= | |
| NM_000074.2:c.633C= , LRG_141t1:c.633C= | NP_000065.1:p.Thr211= | |
| NM_000074.3:c.633C= MANE Select | NP_000065.1:p.Thr211= |