Linked Data
dbSNP Id:
rs756096963
ExAC:
12:50344763 G / A
gnomAD v2:
12-50344763-G-A
gnomAD v4:
12-49950980-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.49950980G>A , CM000674.2:g.49950980G>A | GRCh38 |
| NC_000012.11:g.50344763G>A , CM000674.1:g.50344763G>A | GRCh37 |
| NC_000012.10:g.48631030G>A | NCBI36 |
| NG_008913.1:g.5240G>A , LRG_717:g.5240G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000199280.4:c.150G>A MANE Select | ENSP00000199280.3:p.Leu50= | |
| ENST00000199280.3:c.150G>A | ENSP00000199280.3:p.Leu50= | |
| ENST00000550862.1:c.150G>A | ENSP00000450022.1:p.Leu50= | |
| ENST00000551526.5:c.150G>A | ENSP00000447148.1:p.Leu50= | |
| NM_000486.5:c.150G>A , LRG_717t1:c.150G>A | NP_000477.1:p.Leu50= | |
| NM_000486.6:c.150G>A MANE Select | NP_000477.1:p.Leu50= |