Linked Data
gnomAD v4:
6-33005742-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.33005742T>C , CM000668.2:g.33005742T>C | GRCh38 |
| NC_000006.11:g.32973519T>C , CM000668.1:g.32973519T>C | GRCh37 |
| NC_000006.10:g.33081497T>C | NCBI36 |
| NG_012007.1:g.8871A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000229829.7:c.*1096A>G MANE Select | ENSP00000229829.3:n.*1096A>G | |
| ENST00000229829.6:c.*1096A>G | ENSP00000229829.3:n.*1096A>G | |
| NM_002119.3:c.*1096A>G | NP_002110.1:n.*1096A>G | |
| NM_002119.4:c.*1096A>G MANE Select | NP_002110.1:n.*1096A>G |