Linked Data
gnomAD v4:
14-20892212-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.20892212T>C , CM000676.2:g.20892212T>C | GRCh38 |
| NC_000014.8:g.21360371T>C , CM000676.1:g.21360371T>C | GRCh37 |
| NC_000014.7:g.20430211T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000304639.4:c.*43T>C MANE Select | ENSP00000302324.3:n.*43T>C | |
| ENST00000304639.3:c.*43T>C | ENSP00000302324.3:n.*43T>C | |
| NM_002935.2:c.*43T>C | NP_002926.2:n.*43T>C | |
| XR_110261.2:n.209-16469A>G | ||
| XR_110261.3:n.726-16469A>G | ||
| NM_002935.3:c.*43T>C MANE Select | NP_002926.2:n.*43T>C |