Linked Data
MyVariant Identifiers:
chr6:g.6145879C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.6145646C>G , CM000668.2:g.6145646C>G | GRCh38 |
| NC_000006.11:g.6145879C>G , CM000668.1:g.6145879C>G | GRCh37 |
| NC_000006.10:g.6090878C>G | NCBI36 |
| NG_008107.1:g.180046G>C , LRG_549:g.180046G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264870.8:c.2172G>C MANE Select | ENSP00000264870.3:p.Val724= | |
| ENST00000264870.7:c.2172G>C | ENSP00000264870.3:p.Val724= | |
| NM_000129.3:c.2172G>C , LRG_549t1:c.2172G>C | NP_000120.2:p.Val724= | |
| XM_006715010.2:c.2172G>C | XP_006715073.1:p.Val724= | |
| XM_011514342.1:c.2334G>C | XP_011512644.1:p.Val778= | |
| NM_000129.4:c.2172G>C MANE Select | NP_000120.2:p.Val724= |