Linked Data
MyVariant Identifiers:
chr1:g.196965022T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.196995892T>G , CM000663.2:g.196995892T>G | GRCh38 |
| NC_000001.10:g.196965022T>G , CM000663.1:g.196965022T>G | GRCh37 |
| NC_000001.9:g.195231645T>G | NCBI36 |
| NG_016365.1:g.23356T>G , LRG_227:g.23356T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000699466.1:c.528T>G | ENSP00000514393.1:p.Thr176= | |
| ENST00000699467.1:n.852T>G | ||
| ENST00000699468.1:c.-24-222T>G | ENSP00000514394.1:n.-24-222T>G | |
| ENST00000256785.5:c.783T>G MANE Select | ENSP00000256785.4:p.Thr261= | |
| ENST00000256785.4:c.783T>G | ENSP00000256785.4:p.Thr261= | |
| NM_030787.3:c.783T>G , LRG_227t1:c.783T>G | NP_110414.1:p.Thr261= | |
| XM_011510020.1:c.792T>G | XP_011508322.1:p.Thr264= | |
| XM_011510020.2:c.792T>G | XP_011508322.1:p.Thr264= | |
| NM_030787.4:c.783T>G MANE Select | NP_110414.1:p.Thr261= |