Linked Data
MyVariant Identifiers:
chr11:g.70052249A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.70206143A>T , CM000673.2:g.70206143A>T | GRCh38 |
| NC_000011.9:g.70052249A>T , CM000673.1:g.70052249A>T | GRCh37 |
| NC_000011.8:g.69729897A>T | NCBI36 |
| NG_027966.1:g.7981A>T , LRG_228:g.7981A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301838.5:c.297A>T MANE Select | ENSP00000301838.5:p.Ala99= | |
| ENST00000301838.4:c.297A>T | ENSP00000301838.4:p.Ala99= | |
| NM_003824.3:c.297A>T , LRG_228t1:c.297A>T | NP_003815.1:p.Ala99= | |
| NM_003824.4:c.297A>T MANE Select | NP_003815.1:p.Ala99= |