Linked Data
gnomAD v4:
12-21196898-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.21196898T>C , CM000674.2:g.21196898T>C | GRCh38 |
| NC_000012.11:g.21349832T>C , CM000674.1:g.21349832T>C | GRCh37 |
| NC_000012.10:g.21241099T>C | NCBI36 |
| NG_011745.1:g.70705T>C , LRG_1022:g.70705T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000256958.3:c.728-48T>C MANE Select | ENSP00000256958.2:n.728-48T>C | |
| ENST00000256958.2:c.728-48T>C | ENSP00000256958.2:n.728-48T>C | |
| NM_006446.4:c.728-48T>C , LRG_1022t1:c.728-48T>C | NP_006437.3:n.728-48T>C | |
| NM_006446.5:c.728-48T>C MANE Select | NP_006437.3:n.728-48T>C |