Linked Data
gnomAD v4:
3-81646389-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.81646389T>C , CM000665.2:g.81646389T>C | GRCh38 |
| NC_000003.11:g.81695540T>C , CM000665.1:g.81695540T>C | GRCh37 |
| NC_000003.10:g.81778230T>C | NCBI36 |
| NG_011810.1:g.120412A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000429644.7:c.782+3A>G MANE Select | ENSP00000410833.2:n.782+3A>G | |
| ENST00000429644.6:c.782+3A>G | ENSP00000410833.2:n.782+3A>G | |
| ENST00000489715.1:c.659+3A>G | ENSP00000419638.1:n.659+3A>G | |
| ENST00000498468.1:n.332+3A>G | ||
| NM_000158.3:c.782+3A>G | NP_000149.3:n.782+3A>G | |
| NM_000158.4:c.782+3A>G MANE Select | NP_000149.4:n.782+3A>G |