Linked Data
dbSNP Id:
rs1731632325
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.67740255A>T , CM000666.2:g.67740255A>T | GRCh38 |
| NC_000004.11:g.68605973A>T , CM000666.1:g.68605973A>T | GRCh37 |
| NC_000004.10:g.68288568A>T | NCBI36 |
| NG_009293.1:g.20832T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000226413.5:c.*225T>A MANE Select | ENSP00000226413.5:n.*225T>A | |
| ENST00000226413.4:c.*225T>A | ENSP00000226413.4:n.*225T>A | |
| NM_000406.2:c.*225T>A | NP_000397.1:n.*225T>A | |
| NM_001012763.1:c.*334T>A | NP_001012781.1:n.*334T>A | |
| NM_000406.3:c.*225T>A MANE Select | NP_000397.1:n.*225T>A | |
| NM_001012763.2:c.*334T>A | NP_001012781.1:n.*334T>A |