Linked Data
dbSNP Id:
rs1204642922
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.111222811G>T , CM000668.2:g.111222811G>T | GRCh38 |
| NC_000006.11:g.111544014G>T , CM000668.1:g.111544014G>T | GRCh37 |
| NC_000006.10:g.111650707G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368851.10:c.*576G>T MANE Select | ENSP00000357844.4:n.*576G>T | |
| ENST00000368850.4:c.*576G>T | ENSP00000357843.1:n.*576G>T | |
| ENST00000368851.9:c.*576G>T | ENSP00000357844.4:n.*576G>T | |
| NM_018593.4:c.*576G>T | NP_061063.2:n.*576G>T | |
| XM_005266818.2:c.*530G>T | XP_005266875.1:n.*530G>T | |
| XM_017010237.1:c.*576G>T | XP_016865726.1:n.*576G>T | |
| XR_001743158.1:n.2406G>T | ||
| NM_018593.5:c.*576G>T MANE Select | NP_061063.2:n.*576G>T |