Linked Data
dbSNP Id:
rs1768925437
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.35823883T>C , CM000668.2:g.35823883T>C | GRCh38 |
| NC_000006.11:g.35791660T>C , CM000668.1:g.35791660T>C | GRCh37 |
| NC_000006.10:g.35899638T>C | NCBI36 |
| NG_012184.1:g.23590T>C | |
| NG_012184.2:g.23590T>C | |
| NG_012184.3:g.31678T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360215.3:c.*918T>C MANE Select | ENSP00000353346.1:n.*918T>C | |
| ENST00000496656.2:n.578+4063T>C | ||
| ENST00000651132.1:c.*918T>C | ENSP00000498322.1:n.*918T>C | |
| ENST00000651676.1:c.*16+4420T>C | ENSP00000498699.1:n.*16+4420T>C | |
| ENST00000652718.1:c.508+4420T>C | ENSP00000498866.1:n.508+4420T>C | |
| ENST00000360215.2:c.*918T>C | ENSP00000353346.1:n.*918T>C | |
| ENST00000496656.1:n.812+4063T>C | ||
| NM_182548.3:c.*918T>C | NP_872354.1:n.*918T>C | |
| NM_182548.4:c.*918T>C MANE Select | NP_872354.1:n.*918T>C |