Linked Data
MyVariant Identifiers:
chr12:g.52882207C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52488423C>G , CM000674.2:g.52488423C>G | GRCh38 |
| NC_000012.11:g.52882207C>G , CM000674.1:g.52882207C>G | GRCh37 |
| NC_000012.10:g.51168474C>G | NCBI36 |
| NG_008298.1:g.9975G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000330722.7:c.1329G>C MANE Select | ENSP00000369317.3:p.Arg443= | |
| ENST00000330722.6:c.1329G>C | ENSP00000369317.3:p.Arg443= | |
| NM_005554.3:c.1329G>C | NP_005545.1:p.Arg443= | |
| NM_005554.4:c.1329G>C MANE Select | NP_005545.1:p.Arg443= |