Linked Data
MyVariant Identifiers:
chr12:g.52913886G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52520102G>T , CM000674.2:g.52520102G>T | GRCh38 |
| NC_000012.11:g.52913886G>T , CM000674.1:g.52913886G>T | GRCh37 |
| NC_000012.10:g.51200153G>T | NCBI36 |
| NG_008297.1:g.5358C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252242.9:c.195C>A MANE Select | ENSP00000252242.4:p.Leu65= | |
| ENST00000252242.8:c.195C>A | ENSP00000252242.4:p.Leu65= | |
| ENST00000546577.1:c.195C>A | ENSP00000449651.1:p.Leu65= | |
| ENST00000549420.1:c.43+152C>A | ENSP00000447209.1:n.43+152C>A | |
| ENST00000551275.1:c.172+23C>A | ENSP00000448041.1:n.172+23C>A | |
| ENST00000552629.5:n.293C>A | ||
| NM_000424.3:c.195C>A | NP_000415.2:p.Leu65= | |
| NM_000424.4:c.195C>A MANE Select | NP_000415.2:p.Leu65= |