Linked Data
gnomAD v4:
1-204190410-C-CT
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.204190410_204190411insT , CM000663.2:g.204190410_204190411insT | GRCh38 |
| NC_000001.10:g.204159538_204159539insT , CM000663.1:g.204159538_204159539insT | GRCh37 |
| NC_000001.9:g.202426161_202426162insT | NCBI36 |
| NG_032151.1:g.11081_11082insA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367194.5:c.*73_*74insA MANE Select | ENSP00000356162.4:n.*73_*74insA | |
| ENST00000367194.4:c.*73_*74insA | ENSP00000356162.4:n.*73_*74insA | |
| NM_002256.3:c.*73_*74insA | NP_002247.3:n.*73_*74insA | |
| XM_011509525.1:c.*73_*74insA | XP_011507827.1:n.*73_*74insA | |
| NM_002256.4:c.*73_*74insA MANE Select | NP_002247.3:n.*73_*74insA |