Linked Data
dbSNP Id:
rs1659439073
gnomAD v3:
1-169526007-T-C
gnomAD v4:
1-169526007-T-C
MyVariant Identifiers:
chr1:g.169495245T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.169526007T>C , CM000663.2:g.169526007T>C | GRCh38 |
| NC_000001.10:g.169495245T>C , CM000663.1:g.169495245T>C | GRCh37 |
| NC_000001.9:g.167761869T>C | NCBI36 |
| NG_011806.1:g.65525A>G , LRG_553:g.65525A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367797.9:c.5610A>G MANE Select | ENSP00000356771.3:p.Lys1870= | |
| ENST00000367796.3:c.5625A>G | ENSP00000356770.3:p.Lys1875= | |
| ENST00000367797.7:c.5610A>G | ENSP00000356771.3:p.Lys1870= | |
| NM_000130.4:c.5610A>G , LRG_553t1:c.5610A>G | NP_000121.2:p.Lys1870= | |
| XM_017000660.2:c.5199A>G | XP_016856149.1:p.Lys1733= | |
| NM_000130.5:c.5610A>G MANE Select | NP_000121.2:p.Lys1870= |