Linked Data
dbSNP Id:
rs1131690877
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48380209G>T , CM000675.2:g.48380209G>T | GRCh38 |
| NC_000013.10:g.48954345G>T , CM000675.1:g.48954345G>T | GRCh37 |
| NC_000013.9:g.47852346G>T | NCBI36 |
| NG_009009.1:g.81463G>T , LRG_517:g.81463G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000267163.6:c.1466G>T MANE Select | ENSP00000267163.4:p.Cys489Phe | |
| ENST00000650461.1:c.1466G>T | ENSP00000497193.1:p.Cys489Phe | |
| ENST00000267163.4:c.1466G>T | ENSP00000267163.4:p.Cys489Phe | |
| NM_000321.2:c.1466G>T , LRG_517t1:c.1466G>T | NP_000312.2:p.Cys489Phe | |
| XM_011535171.1:c.1205G>T | XP_011533473.1:p.Cys402Phe | |
| XM_011535171.2:c.1205G>T | XP_011533473.1:p.Cys402Phe | |
| NM_000321.3:c.1466G>T MANE Select | NP_000312.2:p.Cys489Phe |