Linked Data
gnomAD v4:
1-40097322-C-CT
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.40097322_40097323insT , CM000663.2:g.40097322_40097323insT | GRCh38 |
| NC_000001.10:g.40562994_40562995insT , CM000663.1:g.40562994_40562995insT | GRCh37 |
| NC_000001.9:g.40335581_40335582insT | NCBI36 |
| NG_009192.1:g.5148_5149insA , LRG_690:g.5148_5149insA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000433473.7:c.-85_-84insA | ENSP00000394863.3:n.-85_-84insA | |
| NM_000310.3:c.-85_-84insA , LRG_690t1:c.-85_-84insA | NP_000301.1:n.-85_-84insA | |
| NM_001142604.1:c.-85_-84insA | NP_001136076.1:n.-85_-84insA | |
| NM_001363695.1:c.-85_-84insA | NP_001350624.1:n.-85_-84insA |