Linked Data
gnomAD v4:
1-45500213-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.45500213T>C , CM000663.2:g.45500213T>C | GRCh38 |
| NC_000001.10:g.45965885T>C , CM000663.1:g.45965885T>C | GRCh37 |
| NC_000001.9:g.45738472T>C | NCBI36 |
| NG_013378.1:g.5030T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000401061.8:c.-120T>C | ENSP00000383840.4:n.-120T>C | |
| NM_015506.2:c.-120T>C | NP_056321.2:n.-120T>C | |
| NM_001330540.1:c.-342T>C | NP_001317469.1:n.-342T>C |