Linked Data
gnomAD v4:
12-63146838-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.63146838T>C , CM000674.2:g.63146838T>C | GRCh38 |
| NC_000012.11:g.63540618T>C , CM000674.1:g.63540618T>C | GRCh37 |
| NC_000012.10:g.61826885T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000299178.4:c.*521A>G MANE Select | ENSP00000299178.3:n.*521A>G | |
| ENST00000299178.3:c.*521A>G | ENSP00000299178.2:n.*521A>G | |
| ENST00000550940.1:c.538+583A>G | ENSP00000449822.1:n.538+583A>G | |
| NM_000706.4:c.*521A>G | NP_000697.1:n.*521A>G | |
| XM_005269002.3:c.*521A>G | XP_005269059.1:n.*521A>G | |
| NM_000706.5:c.*521A>G MANE Select | NP_000697.1:n.*521A>G |