Linked Data
MyVariant Identifiers:
chr7:g.107330625G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.107690180G>C , CM000669.2:g.107690180G>C | GRCh38 |
| NC_000007.13:g.107330625G>C , CM000669.1:g.107330625G>C | GRCh37 |
| NC_000007.12:g.107117861G>C | NCBI36 |
| NG_008489.1:g.34546G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000644269.2:c.1206G>C MANE Select | ENSP00000494017.1:p.Val402= | |
| ENST00000265715.7:c.1206G>C | ENSP00000265715.3:p.Val402= | |
| NM_000441.1:c.1206G>C | NP_000432.1:p.Val402= | |
| XM_005250425.1:c.1206G>C | XP_005250482.1:p.Val402= | |
| XM_006716025.2:c.1206G>C | XP_006716088.1:p.Val402= | |
| XM_005250425.2:c.1206G>C | XP_005250482.1:p.Val402= | |
| XM_006716025.3:c.1206G>C | XP_006716088.1:p.Val402= | |
| XM_017012318.1:c.1206G>C | XP_016867807.1:p.Val402= | |
| NM_000441.2:c.1206G>C MANE Select | NP_000432.1:p.Val402= |