Linked Data
gnomAD v4:
7-129213223-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.129213223G>C , CM000669.2:g.129213223G>C | GRCh38 |
| NC_000007.13:g.128853064G>C , CM000669.1:g.128853064G>C | GRCh37 |
| NC_000007.12:g.128640300G>C | NCBI36 |
| NG_023340.1:g.29352G>C | |
| NG_023340.2:g.29352G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000249373.8:c.*772G>C MANE Select | ENSP00000249373.3:n.*772G>C | |
| ENST00000655644.1:c.*2891G>C | ENSP00000499377.1:n.*2891G>C | |
| ENST00000249373.7:c.*772G>C | ENSP00000249373.3:n.*772G>C | |
| NM_005631.4:c.*772G>C | NP_005622.1:n.*772G>C | |
| XM_011516522.1:c.*772G>C | XP_011514824.1:n.*772G>C | |
| XM_024446891.1:c.*772G>C | XP_024302659.1:n.*772G>C | |
| NM_005631.5:c.*772G>C MANE Select | NP_005622.1:n.*772G>C |