Linked Data
gnomAD v4:
2-43887002-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.43887002T>C , CM000664.2:g.43887002T>C | GRCh38 |
| NC_000002.11:g.44114141T>C , CM000664.1:g.44114141T>C | GRCh37 |
| NC_000002.10:g.43967645T>C | NCBI36 |
| NG_008247.1:g.114004A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682612.1:c.2550A>G | ||
| ENST00000684454.1:n.9647A>G | ||
| ENST00000260665.12:c.*1598A>G MANE Select | ENSP00000260665.7:n.*1598A>G | |
| ENST00000260665.11:c.*1598A>G | ENSP00000260665.7:n.*1598A>G | |
| NM_133259.3:c.*1598A>G | NP_573566.2:n.*1598A>G | |
| XR_002958896.1:n.5965A>G | ||
| NM_133259.4:c.*1598A>G MANE Select | NP_573566.2:n.*1598A>G |