Linked Data
gnomAD v4:
1-94418466-TA-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94418467del , CM000663.2:g.94418467del | GRCh38 |
| NC_000001.10:g.94884023del , CM000663.1:g.94884023del | GRCh37 |
| NC_000001.9:g.94656611del | NCBI36 |
| NG_008865.1:g.5091del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370214.9:c.-12del MANE Select | ENSP00000359233.4:n.-12del | |
| ENST00000647998.2:c.-12del | ENSP00000497921.2:n.-12del | |
| ENST00000370214.8:c.-12del | ENSP00000359233.4:n.-12del | |
| NM_001122674.1:c.-12del | NP_001116146.1:n.-12del | |
| NM_002858.3:c.-12del | NP_002849.1:n.-12del | |
| XM_006710802.2:c.-12del | XP_006710865.2:n.-12del | |
| NM_002858.4:c.-12del MANE Select | NP_002849.1:n.-12del | |
| NM_001122674.2:c.-12del | NP_001116146.1:n.-12del |