Linked Data
gnomAD v4:
6-33004639-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.33004639G>T , CM000668.2:g.33004639G>T | GRCh38 |
| NC_000006.11:g.32972416G>T , CM000668.1:g.32972416G>T | GRCh37 |
| NC_000006.10:g.33080394G>T | NCBI36 |
| NG_012007.1:g.9974C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000229829.7:c.*2199C>A MANE Select | ENSP00000229829.3:n.*2199C>A | |
| ENST00000229829.6:c.*2199C>A | ENSP00000229829.3:n.*2199C>A | |
| NM_002119.3:c.*2199C>A | NP_002110.1:n.*2199C>A | |
| NM_002119.4:c.*2199C>A MANE Select | NP_002110.1:n.*2199C>A |