Linked Data
dbSNP Id:
rs1601948148
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.25012746T>G , CM000685.2:g.25012746T>G | GRCh38 |
| NC_000023.10:g.25030863T>G , CM000685.1:g.25030863T>G | GRCh37 |
| NC_000023.9:g.24940784T>G | NCBI36 |
| NG_008281.1:g.8203A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000379044.5:c.1073+176A>C MANE Select | ENSP00000368332.4:n.1073+176A>C | |
| ENST00000379044.4:c.1073+176A>C | ENSP00000368332.4:n.1073+176A>C | |
| NM_139058.2:c.1073+176A>C | NP_620689.1:n.1073+176A>C | |
| NM_139058.3:c.1073+176A>C MANE Select | NP_620689.1:n.1073+176A>C |