Linked Data
dbSNP Id:
rs2056202490
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.56983386T>C , CM000678.2:g.56983386T>C | GRCh38 |
| NC_000016.9:g.57017298T>C , CM000678.1:g.57017298T>C | GRCh37 |
| NC_000016.8:g.55574799T>C | NCBI36 |
| NG_008952.1:g.26464T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000200676.8:c.1382T>C MANE Select | ENSP00000200676.3:p.Ile461Thr | |
| ENST00000650358.1:n.1780T>C | ||
| ENST00000200676.7:c.1382T>C | ENSP00000200676.3:p.Ile461Thr | |
| ENST00000379780.6:c.1202T>C | ENSP00000369106.2:p.Ile401Thr | |
| ENST00000566128.1:c.1187T>C | ENSP00000456276.1:p.Ile396Thr | |
| NM_000078.2:c.1382T>C | NP_000069.2:p.Ile461Thr | |
| NM_001286085.1:c.1202T>C | NP_001273014.1:p.Ile401Thr | |
| NM_000078.3:c.1382T>C MANE Select | NP_000069.2:p.Ile461Thr | |
| NM_001286085.2:c.1202T>C | NP_001273014.1:p.Ile401Thr |