Linked Data
MyVariant Identifiers:
chr8:g.97172511T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.96160283T>C , CM000670.2:g.96160283T>C | GRCh38 |
| NC_000008.10:g.97172511T>C , CM000670.1:g.97172511T>C | GRCh37 |
| NC_000008.9:g.97241687T>C | NCBI36 |
| NG_008981.1:g.5510A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000287020.7:c.406+4A>G MANE Select | ENSP00000287020.4:n.406+4A>G | |
| ENST00000287020.6:c.406+4A>G | ENSP00000287020.4:n.406+4A>G | |
| ENST00000620978.1:c.406+4A>G | ENSP00000480170.1:n.406+4A>G | |
| ENST00000621429.1:c.406+4A>G | ENSP00000483711.1:n.406+4A>G | |
| NM_001001557.2:c.406+4A>G | NP_001001557.1:n.406+4A>G | |
| NM_001001557.3:c.406+4A>G | NP_001001557.1:n.406+4A>G | |
| NM_001001557.4:c.406+4A>G MANE Select | NP_001001557.1:n.406+4A>G |