Linked Data
dbSNP Id:
rs9332239
ExAC:
10:96748777 C / T
gnomAD v2:
10-96748777-C-T
gnomAD v3:
10-94989020-C-T
gnomAD v4:
10-94989020-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94989020C>T , CM000672.2:g.94989020C>T | GRCh38 |
| NC_000010.10:g.96748777C>T , CM000672.1:g.96748777C>T | GRCh37 |
| NC_000010.9:g.96738767C>T | NCBI36 |
| NG_008385.1:g.55363C>T | |
| NG_008385.2:g.55863C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000260682.8:c.1465C>T MANE Select | ENSP00000260682.6:p.Pro489Ser | |
| ENST00000643112.1:c.*474C>T | ENSP00000496202.1:n.*474C>T | |
| ENST00000260682.6:c.1465C>T | ENSP00000260682.6:p.Pro489Ser | |
| NM_000771.3:c.1465C>T | NP_000762.2:p.Pro489Ser | |
| NM_000771.4:c.1465C>T MANE Select | NP_000762.2:p.Pro489Ser |