Linked Data
dbSNP Id:
rs1955906140
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.63577237C>T , CM000672.2:g.63577237C>T | GRCh38 |
| NC_000010.10:g.65336997C>T , CM000672.1:g.65336997C>T | GRCh37 |
| NC_000010.9:g.65007003C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373758.5:c.105+10827C>T MANE Select | ENSP00000362863.4:n.105+10827C>T | |
| ENST00000373758.4:c.105+10827C>T | ENSP00000362863.4:n.105+10827C>T | |
| NM_001001330.2:c.105+10827C>T | NP_001001330.1:n.105+10827C>T | |
| XM_011539501.1:c.105+10827C>T | XP_011537803.1:n.105+10827C>T | |
| XM_011539501.2:c.105+10827C>T | XP_011537803.1:n.105+10827C>T | |
| XM_017015896.1:c.105+10827C>T | XP_016871385.1:n.105+10827C>T | |
| NM_001001330.3:c.105+10827C>T MANE Select | NP_001001330.1:n.105+10827C>T |