Linked Data
ClinVar Variation Id:
1201249
ClinVar RCV Id:
RCV001566535
dbSNP Id:
rs116128787
gnomAD v2:
3-10191377-T-A
gnomAD v3:
3-10149693-T-A
gnomAD v4:
3-10149693-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.10149693T>A , CM000665.2:g.10149693T>A | GRCh38 |
| NC_000003.11:g.10191377T>A , CM000665.1:g.10191377T>A | GRCh37 |
| NC_000003.10:g.10166377T>A | NCBI36 |
| NG_008212.3:g.13059T>A , LRG_322:g.13059T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696142.1:c.*141-94T>A | ENSP00000512434.1:n.*141-94T>A | |
| ENST00000696143.1:c.600-94T>A | ENSP00000512435.1:n.600-94T>A | |
| ENST00000696153.1:c.575-94T>A | ENSP00000512444.1:n.575-94T>A | |
| ENST00000256474.3:c.464-94T>A MANE Select | ENSP00000256474.3:n.464-94T>A | |
| ENST00000256474.2:c.464-94T>A | ENSP00000256474.2:n.464-94T>A | |
| ENST00000345392.2:c.341-94T>A | ENSP00000344757.2:n.341-94T>A | |
| ENST00000477538.1:n.600-94T>A | ||
| NM_000551.3:c.464-94T>A , LRG_322t1:c.464-94T>A | NP_000542.1:n.464-94T>A | |
| NM_198156.2:c.341-94T>A | NP_937799.1:n.341-94T>A | |
| NM_001354723.1:c.*18-94T>A | NP_001341652.1:n.*18-94T>A | |
| NM_000551.4:c.464-94T>A MANE Select | NP_000542.1:n.464-94T>A | |
| NM_001354723.2:c.*18-94T>A | NP_001341652.1:n.*18-94T>A | |
| NM_198156.3:c.341-94T>A | NP_937799.1:n.341-94T>A |