ClinVar RCV:
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.151405064A>G , CM000685.2:g.151405064A>G | GRCh38 |
| NC_000023.10:g.150573536A>G , CM000685.1:g.150573536A>G | GRCh37 |
| NC_000023.9:g.150324194A>G | NCBI36 |
| NG_016761.1:g.12880A>G , LRG_860:g.12880A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000330374.7:c.*6A>G MANE Select | ENSP00000333255.6:n.*6A>G | |
| ENST00000330374.6:c.*6A>G | ENSP00000333255.6:n.*6A>G | |
| ENST00000370361.5:c.*6A>G | ENSP00000359386.1:n.*6A>G | |
| ENST00000477649.1:n.392A>G | ||
| NM_001017980.3:c.*6A>G , LRG_860t1:c.*6A>G | NP_001017980.1:n.*6A>G | |
| XM_011531125.1:c.*6A>G | XP_011529427.1:n.*6A>G | |
| NM_001363810.1:c.*6A>G | NP_001350739.1:n.*6A>G | |
| NM_001017980.4:c.*6A>G MANE Select | NP_001017980.1:n.*6A>G |