Linked Data
dbSNP Id:
rs1721629257
gnomAD v3:
4-99420638-A-G
gnomAD v4:
4-99420638-A-G
MyVariant Identifiers:
chr4:g.100341795A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.99420638A>G , CM000666.2:g.99420638A>G | GRCh38 |
| NC_000004.11:g.100341795A>G , CM000666.1:g.100341795A>G | GRCh37 |
| NC_000004.10:g.100560818A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000437033.7:c.720T>C MANE Select | ENSP00000414254.2:p.Cys240= | |
| ENST00000209665.8:c.756T>C | ENSP00000209665.4:p.Cys252= | |
| ENST00000437033.6:c.720T>C | ENSP00000414254.2:p.Cys240= | |
| ENST00000476959.5:c.780T>C | ENSP00000420269.1:p.Cys260= | |
| ENST00000482593.5:c.549T>C | ENSP00000420613.1:p.Cys183= | |
| NM_000673.4:c.756T>C | NP_000664.2:p.Cys252= | |
| NM_001166504.1:c.780T>C | NP_001159976.1:p.Cys260= | |
| NM_000673.7:c.720T>C MANE Select | NP_000664.3:p.Cys240= | |
| NM_001166504.2:c.780T>C | NP_001159976.1:p.Cys260= |