Linked Data
gnomAD v4:
1-197039196-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.197039196C>A , CM000663.2:g.197039196C>A | GRCh38 |
| NC_000001.10:g.197008326C>A , CM000663.1:g.197008326C>A | GRCh37 |
| NC_000001.9:g.195274949C>A | NCBI36 |
| NG_012065.1:g.33072G>T , LRG_550:g.33072G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367412.2:c.*182G>T MANE Select | ENSP00000356382.2:n.*182G>T | |
| ENST00000649282.1:c.923G>T | ENSP00000497116.1:n.923G>T | |
| ENST00000367412.1:c.*182G>T | ENSP00000356382.1:n.*182G>T | |
| NM_001994.2:c.*182G>T , LRG_550t1:c.*182G>T | NP_001985.2:n.*182G>T | |
| XM_011509283.2:c.*1103G>T | XP_011507585.1:n.*1103G>T | |
| XM_011509284.2:c.*1103G>T | XP_011507586.1:n.*1103G>T | |
| XM_011509286.2:c.*1103G>T | XP_011507588.1:n.*1103G>T | |
| NM_001994.3:c.*182G>T MANE Select | NP_001985.2:n.*182G>T |