Linked Data
ClinVar Variation Id:
287739
dbSNP Id:
rs201822027
ExAC:
2:20137662 A / C
gnomAD v2:
2-20137662-A-C
gnomAD v3:
2-19937901-A-C
gnomAD v4:
2-19937901-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.19937901A>C , CM000664.2:g.19937901A>C | GRCh38 |
| NC_000002.11:g.20137662A>C , CM000664.1:g.20137662A>C | GRCh37 |
| NC_000002.10:g.20001143A>C | NCBI36 |
| NG_021212.1:g.57223T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000281405.9:c.2109T>G MANE Select | ENSP00000281405.5:p.Thr703= | |
| ENST00000345530.8:c.2142T>G MANE Plus Clinical | ENSP00000314444.5:p.Thr714= | |
| ENST00000281405.8:c.2109T>G | ENSP00000281405.4:p.Thr703= | |
| ENST00000345530.7:c.2142T>G | ENSP00000314444.5:p.Thr714= | |
| ENST00000414212.5:c.2142T>G | ENSP00000390802.1:p.Thr714= | |
| ENST00000445063.5:c.1585T>G | ||
| ENST00000453014.1:c.747T>G | ENSP00000404409.1:p.Thr249= | |
| NM_001006657.1:c.2142T>G | NP_001006658.1:p.Thr714= | |
| NM_020779.3:c.2109T>G | NP_065830.2:p.Thr703= | |
| XM_011533007.1:c.837T>G | XP_011531309.1:p.Thr279= | |
| XR_426989.2:n.2142T>G | ||
| XM_011533007.2:c.837T>G | XP_011531309.1:p.Thr279= | |
| XR_001738862.1:n.2086T>G | ||
| XR_426989.3:n.2142T>G | ||
| NM_001006657.2:c.2142T>G MANE Plus Clinical | NP_001006658.1:p.Thr714= | |
| NM_020779.4:c.2109T>G MANE Select | NP_065830.2:p.Thr703= |