Linked Data
dbSNP Id:
rs772159414
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94781955C>T , CM000672.2:g.94781955C>T | GRCh38 |
| NC_000010.10:g.96541712C>T , CM000672.1:g.96541712C>T | GRCh37 |
| NC_000010.9:g.96531702C>T | NCBI36 |
| NG_008384.2:g.24250C>T | |
| NG_008384.3:g.24275C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371321.9:c.777C>T MANE Select | ENSP00000360372.3:p.Asn259= | |
| ENST00000645461.1:n.1830C>T | ||
| ENST00000371321.7:c.777C>T | ENSP00000360372.3:p.Asn259= | |
| ENST00000464755.1:c.1540C>T | ENSP00000483243.1:n.1540C>T | |
| NM_000769.2:c.777C>T | NP_000760.1:p.Asn259= | |
| NM_000769.4:c.777C>T MANE Select | NP_000760.1:p.Asn259= |