Linked Data
gnomAD v4:
2-73640800-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.73640800T>C , CM000664.2:g.73640800T>C | GRCh38 |
| NC_000002.11:g.73867927T>C , CM000664.1:g.73867927T>C | GRCh37 |
| NC_000002.10:g.73721435T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000272425.4:c.*145A>G MANE Select | ENSP00000272425.3:n.*145A>G | |
| NM_003960.3:c.*145A>G | NP_003951.3:n.*145A>G | |
| NM_003960.4:c.*145A>G MANE Select | NP_003951.3:n.*145A>G |