Linked Data
dbSNP Id:
rs2124976577
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.8733360A>G , CM000665.2:g.8733360A>G | GRCh38 |
| NC_000003.11:g.8775046A>G , CM000665.1:g.8775046A>G | GRCh37 |
| NC_000003.10:g.8750046A>G | NCBI36 |
| NG_008797.2:g.4551A>G , LRG_329:g.4551A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000435138.5:c.64+9099T>C | ENSP00000412333.1:n.64+9099T>C | |
| ENST00000478513.1:n.335+9099T>C | ||
| XR_940435.1:n.330+9099T>C | ||
| XM_017006530.1:c.-283+9099T>C | XP_016862019.1:n.-283+9099T>C |