Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.116173474C= , CM000685.2:g.116173474C= | GRCh38 |
| NC_000023.10:g.115304727C= , CM000685.1:g.115304727C= | GRCh37 |
| NC_000023.9:g.115218755C= | NCBI36 |
| NG_016326.1:g.7770C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371906.5:c.*102C= MANE Select | ENSP00000360973.4:n.*102C= | |
| ENST00000371906.4:c.*102C= | ENSP00000360973.4:n.*102C= | |
| NM_000686.4:c.*102C= | NP_000677.2:n.*102C= | |
| XM_011537533.1:c.*102C= | XP_011535835.1:n.*102C= | |
| NM_000686.5:c.*102C= MANE Select | NP_000677.2:n.*102C= | |
| NM_001385624.1:c.*102C= | NP_001372553.1:n.*102C= |