Linked Data
dbSNP Id:
rs2046845472
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.82727262A>C , CM000679.2:g.82727262A>C | GRCh38 |
| NC_000017.10:g.80685138A>C , CM000679.1:g.80685138A>C | GRCh37 |
| NC_000017.9:g.78278427A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000269373.11:c.*91A>C MANE Select | ENSP00000269373.6:n.*91A>C | |
| ENST00000269373.10:c.*91A>C | ENSP00000269373.6:n.*91A>C | |
| ENST00000571594.1:c.53+95A>C | ENSP00000459751.1:n.53+95A>C | |
| ENST00000574832.5:c.*978A>C | ENSP00000460869.1:n.*978A>C | |
| NM_024619.3:c.*91A>C | NP_078895.2:n.*91A>C | |
| NR_046408.1:n.1199A>C | ||
| XM_024450948.1:c.*91A>C | XP_024306716.1:n.*91A>C | |
| NM_024619.4:c.*91A>C MANE Select | NP_078895.2:n.*91A>C | |
| NR_046408.2:n.1199A>C |