Linked Data
dbSNP Id:
rs2070305508
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.11309980C>T , CM000678.2:g.11309980C>T | GRCh38 |
| NC_000016.9:g.11403837C>T , CM000678.1:g.11403837C>T | GRCh37 |
| NC_000016.8:g.11311338C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000649869.1:n.152+60202C>T | ||
| ENST00000572173.1:c.-436-2849C>T | ENSP00000461206.1:n.-436-2849C>T | |
| ENST00000573910.1:n.161-6472C>T | ||
| XR_933070.1:n.733+60202C>T | ||
| XR_933070.3:n.876+60202C>T |