Linked Data
dbSNP Id:
rs2146048725
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.43551566C>A , CM000681.2:g.43551566C>A | GRCh38 |
| NC_000019.9:g.44055718C>A , CM000681.1:g.44055718C>A | GRCh37 |
| NC_000019.8:g.48747558C>A | NCBI36 |
| NG_033799.1:g.29013G>T , LRG_784:g.29013G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262887.10:c.1199+5G>T MANE Select | ENSP00000262887.5:n.1199+5G>T | |
| ENST00000262887.9:c.1199+5G>T | ENSP00000262887.4:n.1199+5G>T | |
| ENST00000543982.5:c.1106+5G>T | ENSP00000443671.1:n.1106+5G>T | |
| NM_006297.2:c.1199+5G>T , LRG_784t1:c.1199+5G>T | NP_006288.2:n.1199+5G>T | |
| NM_006297.3:c.1199+5G>T MANE Select | NP_006288.2:n.1199+5G>T |