Linked Data
MyVariant Identifiers:
chr6:g.121768659C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.121447513C>G , CM000668.2:g.121447513C>G | GRCh38 |
| NC_000006.11:g.121768659C>G , CM000668.1:g.121768659C>G | GRCh37 |
| NC_000006.10:g.121810358C>G | NCBI36 |
| NG_008308.1:g.16915C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000282561.4:c.666C>G MANE Select | ENSP00000282561.3:p.Ala222= | |
| ENST00000647564.1:c.666C>G | ENSP00000497565.1:p.Ala222= | |
| ENST00000649003.1:c.666C>G | ENSP00000497283.1:p.Ala222= | |
| ENST00000650427.1:c.666C>G | ENSP00000497367.1:p.Ala222= | |
| ENST00000282561.3:c.666C>G | ENSP00000282561.3:p.Ala222= | |
| NM_000165.4:c.666C>G | NP_000156.1:p.Ala222= | |
| NM_000165.5:c.666C>G MANE Select | NP_000156.1:p.Ala222= |