Linked Data
dbSNP Id:
rs2148307195
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.29717573C>T , CM000664.2:g.29717573C>T | GRCh38 |
| NC_000002.11:g.29940439C>T , CM000664.1:g.29940439C>T | GRCh37 |
| NC_000002.10:g.29793943C>T | NCBI36 |
| NG_009445.1:g.208994G>A , LRG_488:g.208994G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000389048.8:c.787+5G>A MANE Select | ENSP00000373700.3:n.787+5G>A | |
| ENST00000389048.7:c.787+5G>A | ENSP00000373700.3:n.787+5G>A | |
| ENST00000618119.4:c.-345+5G>A | ENSP00000482733.1:n.-345+5G>A | |
| NM_004304.4:c.787+5G>A | NP_004295.2:n.787+5G>A | |
| XR_001738688.2:n.1717+5G>A | ||
| NM_004304.5:c.787+5G>A MANE Select | NP_004295.2:n.787+5G>A |