Linked Data
MyVariant Identifiers:
chr12:g.89744557A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.89350780A>G , CM000674.2:g.89350780A>G | GRCh38 |
| NC_000012.11:g.89744557A>G , CM000674.1:g.89744557A>G | GRCh37 |
| NC_000012.10:g.88268688A>G | NCBI36 |
| NG_033915.1:g.7080T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000279488.8:c.646T>C MANE Select | ENSP00000279488.6:p.Leu216= | |
| ENST00000279488.7:c.646T>C | ENSP00000279488.6:p.Leu216= | |
| ENST00000308385.6:c.400+860T>C | ENSP00000307835.6:n.400+860T>C | |
| ENST00000547140.1:n.332T>C | ||
| ENST00000547291.1:c.271T>C | ENSP00000449838.1:p.Leu91= | |
| NM_001946.3:c.646T>C | NP_001937.2:p.Leu216= | |
| NM_022652.3:c.400+860T>C | NP_073143.2:n.400+860T>C | |
| NM_001946.4:c.646T>C MANE Select | NP_001937.2:p.Leu216= | |
| NM_022652.4:c.400+860T>C | NP_073143.2:n.400+860T>C |