Linked Data
dbSNP Id:
rs2079618589
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.1103979A>C , CM000681.2:g.1103979A>C | GRCh38 |
| NC_000019.9:g.1103978A>C , CM000681.1:g.1103978A>C | GRCh37 |
| NC_000019.8:g.1054978A>C | NCBI36 |
| NG_050621.1:g.5054A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000354171.12:c.-65A>C | ENSP00000346103.7:n.-65A>C | |
| ENST00000616066.4:c.-65A>C | ENSP00000485000.1:n.-65A>C | |
| NM_001039847.2:c.-65A>C | NP_001034936.1:n.-65A>C | |
| NM_002085.4:c.-65A>C | NP_002076.2:n.-65A>C |