Linked Data
dbSNP Id:
rs1016386177
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.1410566G>T , CM000672.2:g.1410566G>T | GRCh38 |
| NC_000010.10:g.1452761G>T , CM000672.1:g.1452761G>T | GRCh37 |
| NC_000010.9:g.1442761G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381312.6:c.101-31406C>A MANE Select | ENSP00000370713.1:n.101-31406C>A | |
| ENST00000381312.5:c.101-31406C>A | ENSP00000370713.1:n.101-31406C>A | |
| NM_018702.3:c.101-31406C>A | NP_061172.1:n.101-31406C>A | |
| XR_930468.1:n.449-31406C>A | ||
| NM_018702.4:c.101-31406C>A MANE Select | NP_061172.1:n.101-31406C>A |