Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.197039228T>A , CM000663.2:g.197039228T>A | GRCh38 |
| NC_000001.10:g.197008358T>A , CM000663.1:g.197008358T>A | GRCh37 |
| NC_000001.9:g.195274981T>A | NCBI36 |
| NG_012065.1:g.33040A>T , LRG_550:g.33040A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367412.2:c.*150A>T MANE Select | ENSP00000356382.2:n.*150A>T | |
| ENST00000649282.1:c.891A>T | ENSP00000497116.1:n.891A>T | |
| ENST00000367412.1:c.*150A>T | ENSP00000356382.1:n.*150A>T | |
| NM_001994.2:c.*150A>T , LRG_550t1:c.*150A>T | NP_001985.2:n.*150A>T | |
| XM_011509283.2:c.*1071A>T | XP_011507585.1:n.*1071A>T | |
| XM_011509284.2:c.*1071A>T | XP_011507586.1:n.*1071A>T | |
| XM_011509286.2:c.*1071A>T | XP_011507588.1:n.*1071A>T | |
| NM_001994.3:c.*150A>T MANE Select | NP_001985.2:n.*150A>T |