Linked Data
gnomAD v4:
12-69353327-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.69353327T>G , CM000674.2:g.69353327T>G | GRCh38 |
| NC_000012.11:g.69747107T>G , CM000674.1:g.69747107T>G | GRCh37 |
| NC_000012.10:g.68033374T>G | NCBI36 |
| NG_008195.1:g.9974T>G , LRG_768:g.9974T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261267.7:c.*108T>G MANE Select | ENSP00000261267.2:n.*108T>G | |
| ENST00000261267.6:c.*108T>G | ENSP00000261267.2:n.*108T>G | |
| ENST00000549690.1:c.*62T>G | ENSP00000449898.1:n.*62T>G | |
| NM_000239.2:c.*108T>G , LRG_768t1:c.*108T>G | NP_000230.1:n.*108T>G | |
| NM_000239.3:c.*108T>G MANE Select | NP_000230.1:n.*108T>G |