Linked Data
MyVariant Identifiers:
chr1:g.16458574G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.16132079G>C , CM000663.2:g.16132079G>C | GRCh38 |
| NC_000001.10:g.16458574G>C , CM000663.1:g.16458574G>C | GRCh37 |
| NC_000001.9:g.16331161G>C | NCBI36 |
| NG_021396.1:g.29009C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000358432.8:c.2310C>G MANE Select | ENSP00000351209.5:p.Ala770= | |
| ENST00000358432.7:c.2310C>G | ENSP00000351209.5:p.Ala770= | |
| NM_004431.3:c.2310C>G | NP_004422.2:p.Ala770= | |
| NM_001329090.1:c.2148C>G | NP_001316019.1:p.Ala716= | |
| NM_004431.4:c.2310C>G | NP_004422.2:p.Ala770= | |
| NM_004431.5:c.2310C>G MANE Select | NP_004422.2:p.Ala770= | |
| NM_001329090.2:c.2148C>G | NP_001316019.1:p.Ala716= |