Linked Data
gnomAD v4:
22-29313133-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.29313133T>C , CM000684.2:g.29313133T>C | GRCh38 |
| NC_000022.10:g.29709122T>C , CM000684.1:g.29709122T>C | GRCh37 |
| NC_000022.9:g.28039122T>C | NCBI36 |
| NG_032959.1:g.11127T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000216101.7:c.*168A>G MANE Select | ENSP00000216101.6:n.*168A>G | |
| ENST00000216101.6:c.*168A>G | ENSP00000216101.6:n.*168A>G | |
| ENST00000401450.3:c.*726A>G | ENSP00000386095.3:n.*726A>G | |
| NM_006477.4:c.*168A>G | NP_006468.1:n.*168A>G | |
| XM_011529821.1:c.*168A>G | XP_011528123.1:n.*168A>G | |
| XM_011529822.1:c.*168A>G | XP_011528124.1:n.*168A>G | |
| XM_011529823.1:c.*168A>G | XP_011528125.1:n.*168A>G | |
| NM_006477.5:c.*168A>G MANE Select | NP_006468.1:n.*168A>G |