Linked Data
gnomAD v4:
3-81646302-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.81646302C>A , CM000665.2:g.81646302C>A | GRCh38 |
| NC_000003.11:g.81695453C>A , CM000665.1:g.81695453C>A | GRCh37 |
| NC_000003.10:g.81778143C>A | NCBI36 |
| NG_011810.1:g.120499G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000429644.7:c.782+90G>T MANE Select | ENSP00000410833.2:n.782+90G>T | |
| ENST00000429644.6:c.782+90G>T | ENSP00000410833.2:n.782+90G>T | |
| ENST00000489715.1:c.659+90G>T | ENSP00000419638.1:n.659+90G>T | |
| ENST00000498468.1:n.332+90G>T | ||
| NM_000158.3:c.782+90G>T | NP_000149.3:n.782+90G>T | |
| NM_000158.4:c.782+90G>T MANE Select | NP_000149.4:n.782+90G>T |