Linked Data
dbSNP Id:
rs1036602487
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.103086541T>A , CM000672.2:g.103086541T>A | GRCh38 |
| NC_000010.10:g.104846298T>A , CM000672.1:g.104846298T>A | GRCh37 |
| NC_000010.9:g.104836288T>A | NCBI36 |
| NG_042272.1:g.111766A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369878.9:c.*9361T>A MANE Select | ENSP00000358894.3:n.*9361T>A | |
| ENST00000369878.8:c.*9361T>A | ENSP00000358894.3:n.*9361T>A | |
| XR_001747118.1:n.12242T>A | ||
| XR_001747121.1:n.12206T>A | ||
| NM_017649.5:c.*9361T>A MANE Select | NP_060119.3:n.*9361T>A | |
| NM_199076.3:c.*9361T>A | NP_951058.1:n.*9361T>A |