Linked Data
dbSNP Id:
rs1649377446
gnomAD v4:
1-153991222-A-G
MyVariant Identifiers:
chr1:g.153963698A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.153991222A>G , CM000663.2:g.153991222A>G | GRCh38 |
| NC_000001.10:g.153963698A>G , CM000663.1:g.153963698A>G | GRCh37 |
| NC_000001.9:g.152230322A>G | NCBI36 |
| NG_053102.2:g.5468A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000477151.2:n.302A>G | ||
| ENST00000643794.1:c.235A>G | ENSP00000495765.1:p.Arg79Gly | |
| ENST00000651669.1:c.114A>G MANE Select | ENSP00000499044.1:p.Pro38= | |
| ENST00000368567.4:c.114A>G | ENSP00000357555.4:p.Pro38= | |
| ENST00000392558.4:c.114A>G | ENSP00000376341.4:p.Pro38= | |
| ENST00000477151.1:n.269A>G | ||
| ENST00000493224.5:n.380A>G | ||
| NM_001030.4:c.114A>G | NP_001021.1:p.Pro38= | |
| NM_001030.6:c.114A>G MANE Select | NP_001021.1:p.Pro38= | |
| NM_001349946.1:c.18A>G | NP_001336875.1:p.Pro6= | |
| NM_001349947.1:c.18A>G | NP_001336876.1:p.Pro6= | |
| NM_001349946.2:c.18A>G | NP_001336875.1:p.Pro6= | |
| NM_001349947.2:c.18A>G | NP_001336876.1:p.Pro6= |