Linked Data
dbSNP Id:
rs1654953345
gnomAD v3:
1-197039384-T-C
gnomAD v4:
1-197039384-T-C
MyVariant Identifiers:
chr1:g.197008514T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.197039384T>C , CM000663.2:g.197039384T>C | GRCh38 |
| NC_000001.10:g.197008514T>C , CM000663.1:g.197008514T>C | GRCh37 |
| NC_000001.9:g.195275137T>C | NCBI36 |
| NG_012065.1:g.32884A>G , LRG_550:g.32884A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367412.2:c.1980A>G MANE Select | ENSP00000356382.2:p.Arg660= | |
| ENST00000649282.1:c.735A>G | ENSP00000497116.1:p.Arg245= | |
| ENST00000367412.1:c.1980A>G | ENSP00000356382.1:p.Arg660= | |
| NM_001994.2:c.1980A>G , LRG_550t1:c.1980A>G | NP_001985.2:p.Arg660= | |
| XM_011509283.2:c.*915A>G | XP_011507585.1:n.*915A>G | |
| XM_011509284.2:c.*915A>G | XP_011507586.1:n.*915A>G | |
| XM_011509286.2:c.*915A>G | XP_011507588.1:n.*915A>G | |
| NM_001994.3:c.1980A>G MANE Select | NP_001985.2:p.Arg660= |