Linked Data
dbSNP Id:
rs2070041322
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.19961779G>A , CM000670.2:g.19961779G>A | GRCh38 |
| NC_000008.10:g.19819290G>A , CM000670.1:g.19819290G>A | GRCh37 |
| NC_000008.9:g.19863570G>A | NCBI36 |
| NG_008855.1:g.27709G>A | |
| NG_008855.2:g.65063G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650287.1:c.1323-336G>A MANE Select | ENSP00000497642.1:n.1323-336G>A | |
| ENST00000650478.1:c.263-336G>A | ENSP00000497560.1:n.263-336G>A | |
| ENST00000311322.8:c.1323-336G>A | ENSP00000309757.6:n.1323-336G>A | |
| NM_000237.2:c.1323-336G>A | NP_000228.1:n.1323-336G>A | |
| NM_000237.3:c.1323-336G>A MANE Select | NP_000228.1:n.1323-336G>A |