Linked Data
gnomAD v4:
1-197039246-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.197039246G>T , CM000663.2:g.197039246G>T | GRCh38 |
| NC_000001.10:g.197008376G>T , CM000663.1:g.197008376G>T | GRCh37 |
| NC_000001.9:g.195274999G>T | NCBI36 |
| NG_012065.1:g.33022C>A , LRG_550:g.33022C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367412.2:c.*132C>A MANE Select | ENSP00000356382.2:n.*132C>A | |
| ENST00000649282.1:c.873C>A | ENSP00000497116.1:n.873C>A | |
| ENST00000367412.1:c.*132C>A | ENSP00000356382.1:n.*132C>A | |
| NM_001994.2:c.*132C>A , LRG_550t1:c.*132C>A | NP_001985.2:n.*132C>A | |
| XM_011509283.2:c.*1053C>A | XP_011507585.1:n.*1053C>A | |
| XM_011509284.2:c.*1053C>A | XP_011507586.1:n.*1053C>A | |
| XM_011509286.2:c.*1053C>A | XP_011507588.1:n.*1053C>A | |
| NM_001994.3:c.*132C>A MANE Select | NP_001985.2:n.*132C>A |