Linked Data
dbSNP Id:
rs1186781402
gnomAD v4:
7-116771928-A-T
MyVariant Identifiers:
chr7:g.116411982A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.116771928A>T , CM000669.2:g.116771928A>T | GRCh38 |
| NC_000007.13:g.116411982A>T , CM000669.1:g.116411982A>T | GRCh37 |
| NC_000007.12:g.116199218A>T | NCBI36 |
| NG_008996.1:g.104524A>T , LRG_662:g.104524A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000436117.3:c.*572A>T | ENSP00000410980.2:n.*572A>T | |
| ENST00000318493.11:c.3021A>T | ENSP00000317272.6:p.Val1007= | |
| ENST00000397752.8:c.2967A>T MANE Select | ENSP00000380860.3:p.Val989= | |
| ENST00000318493.10:c.3021A>T | ENSP00000317272.6:p.Val1007= | |
| ENST00000397752.7:c.2967A>T | ENSP00000380860.3:p.Val989= | |
| ENST00000454623.1:c.283+274A>T | ENSP00000398140.1:n.283+274A>T | |
| NM_000245.2:c.2967A>T | NP_000236.2:p.Val989= | |
| NM_001127500.1:c.3021A>T , LRG_662t1:c.3021A>T | NP_001120972.1:p.Val1007= | |
| XM_006715990.2:c.1677A>T | XP_006716053.1:p.Val559= | |
| XM_006715991.2:c.1677A>T | XP_006716054.1:p.Val559= | |
| XM_011516223.1:c.3024A>T | XP_011514525.1:p.Val1008= | |
| NM_000245.3:c.2967A>T | NP_000236.2:p.Val989= | |
| NM_001127500.2:c.3021A>T | NP_001120972.1:p.Val1007= | |
| NM_001324402.1:c.1677A>T | NP_001311331.1:p.Val559= | |
| XR_001744772.1:n.3098A>T | ||
| NM_001127500.3:c.3021A>T | NP_001120972.1:p.Val1007= | |
| NM_000245.4:c.2967A>T MANE Select | NP_000236.2:p.Val989= | |
| NM_001324402.2:c.1677A>T | NP_001311331.1:p.Val559= |