Linked Data
MyVariant Identifiers:
chr12:g.5154504C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.5045338C>G , CM000674.2:g.5045338C>G | GRCh38 |
| NC_000012.11:g.5154504C>G , CM000674.1:g.5154504C>G | GRCh37 |
| NC_000012.10:g.5024765C>G | NCBI36 |
| NG_012198.1:g.6420C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252321.5:c.1191C>G MANE Select | ENSP00000252321.3:p.Ala397= | |
| ENST00000252321.4:c.1191C>G | ENSP00000252321.3:p.Ala397= | |
| NM_002234.3:c.1191C>G | NP_002225.2:p.Ala397= | |
| NM_002234.4:c.1191C>G MANE Select | NP_002225.2:p.Ala397= |