Linked Data
gnomAD v4:
10-102503968-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.102503968T>C , CM000672.2:g.102503968T>C | GRCh38 |
| NC_000010.10:g.104263725T>C , CM000672.1:g.104263725T>C | GRCh37 |
| NC_000010.9:g.104253715T>C | NCBI36 |
| NG_011901.1:g.3788A>G | |
| NG_021338.1:g.5007T>C , LRG_521:g.5007T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NM_001178133.1:c.-185T>C | NP_001171604.1:n.-185T>C | |
| NM_016169.3:c.-185T>C , LRG_521t1:c.-185T>C | NP_057253.2:n.-185T>C | |
| XM_011539858.1:c.-185T>C | XP_011538160.1:n.-185T>C | |
| XM_011539859.1:c.-29-156T>C | XP_011538161.1:n.-29-156T>C | |
| XM_011539860.1:c.-185T>C | XP_011538162.1:n.-185T>C | |
| XM_011539863.1:c.8+982T>C | XP_011538165.1:n.8+982T>C | |
| XM_011539863.3:c.8+982T>C | XP_011538165.1:n.8+982T>C |