Linked Data
MyVariant Identifiers:
chr16:g.89245880C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.89179472C>G , CM000678.2:g.89179472C>G | GRCh38 |
| NC_000016.9:g.89245880C>G , CM000678.1:g.89245880C>G | GRCh37 |
| NC_000016.8:g.87773381C>G | NCBI36 |
| NG_012055.1:g.12718C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000289746.3:c.99C>G MANE Select | ENSP00000289746.2:p.Pro33= | |
| ENST00000289746.2:c.99C>G | ENSP00000289746.2:p.Pro33= | |
| ENST00000521087.5:n.164C>G | ||
| ENST00000524089.1:n.164C>G | ||
| NM_004933.2:c.99C>G | NP_004924.1:p.Pro33= | |
| XM_011522806.1:c.99C>G | XP_011521108.1:p.Pro33= | |
| NM_004933.3:c.99C>G MANE Select | NP_004924.1:p.Pro33= |