Linked Data
dbSNP Id:
rs1692104586
gnomAD v3:
2-206144999-A-G
gnomAD v4:
2-206144999-A-G
MyVariant Identifiers:
chr2:g.207009723A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.206144999A>G , CM000664.2:g.206144999A>G | GRCh38 |
| NC_000002.11:g.207009723A>G , CM000664.1:g.207009723A>G | GRCh37 |
| NC_000002.10:g.206717968A>G | NCBI36 |
| NG_009248.1:g.19465T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000233190.11:c.765T>C MANE Select | ENSP00000233190.5:p.Asp255= | |
| ENST00000233190.10:c.765T>C | ENSP00000233190.5:p.Asp255= | |
| ENST00000423725.5:c.594T>C | ENSP00000397760.1:p.Asp198= | |
| ENST00000432169.5:c.432T>C | ENSP00000409689.1:p.Asp144= | |
| ENST00000440274.5:c.657T>C | ENSP00000409766.1:p.Asp219= | |
| ENST00000449699.5:c.765T>C | ENSP00000399912.1:p.Asp255= | |
| ENST00000455934.6:c.807T>C | ENSP00000392709.2:p.Asp269= | |
| ENST00000457011.5:c.417T>C | ENSP00000400976.1:p.Asp139= | |
| NM_001199981.1:c.657T>C | NP_001186910.1:p.Asp219= | |
| NM_001199982.1:c.432T>C | NP_001186911.1:p.Asp144= | |
| NM_001199983.1:c.594T>C | NP_001186912.1:p.Asp198= | |
| NM_001199984.1:c.807T>C | NP_001186913.1:p.Asp269= | |
| NM_005006.6:c.765T>C | NP_004997.4:p.Asp255= | |
| XM_017004188.2:c.6T>C | XP_016859677.1:p.Asp2= | |
| NM_001199981.2:c.657T>C | NP_001186910.1:p.Asp219= | |
| NM_001199982.2:c.432T>C | NP_001186911.1:p.Asp144= | |
| NM_001199983.2:c.594T>C | NP_001186912.1:p.Asp198= | |
| NM_005006.7:c.765T>C MANE Select | NP_004997.4:p.Asp255= | |
| NM_001199984.2:c.807T>C | NP_001186913.1:p.Asp269= |