Linked Data
dbSNP Id:
rs1915105285
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.3159766T>C , CM000681.2:g.3159766T>C | GRCh38 |
| NC_000019.9:g.3159764T>C , CM000681.1:g.3159764T>C | GRCh37 |
| NC_000019.8:g.3110764T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262958.4:c.898+1885T>C MANE Select | ENSP00000262958.2:n.898+1885T>C | |
| ENST00000262958.3:c.898+1885T>C | ENSP00000262958.2:n.898+1885T>C | |
| NM_002068.3:c.898+1885T>C | NP_002059.3:n.898+1885T>C | |
| NM_002068.4:c.898+1885T>C MANE Select | NP_002059.3:n.898+1885T>C |