Linked Data
gnomAD v4:
1-204190415-C-CAA
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.204190415_204190416insAA , CM000663.2:g.204190415_204190416insAA | GRCh38 |
| NC_000001.10:g.204159543_204159544insAA , CM000663.1:g.204159543_204159544insAA | GRCh37 |
| NC_000001.9:g.202426166_202426167insAA | NCBI36 |
| NG_032151.1:g.11076_11077insTT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367194.5:c.*68_*69insTT MANE Select | ENSP00000356162.4:n.*68_*69insTT | |
| ENST00000367194.4:c.*68_*69insTT | ENSP00000356162.4:n.*68_*69insTT | |
| NM_002256.3:c.*68_*69insTT | NP_002247.3:n.*68_*69insTT | |
| XM_011509525.1:c.*68_*69insTT | XP_011507827.1:n.*68_*69insTT | |
| NM_002256.4:c.*68_*69insTT MANE Select | NP_002247.3:n.*68_*69insTT |