Linked Data
MyVariant Identifiers:
chr1:g.196965253A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.196996123A>C , CM000663.2:g.196996123A>C | GRCh38 |
| NC_000001.10:g.196965253A>C , CM000663.1:g.196965253A>C | GRCh37 |
| NC_000001.9:g.195231876A>C | NCBI36 |
| NG_016365.1:g.23587A>C , LRG_227:g.23587A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000699466.1:c.637A>C | ENSP00000514393.1:p.Arg213= | |
| ENST00000699467.1:n.961A>C | ||
| ENST00000699468.1:c.-15A>C | ENSP00000514394.1:n.-15A>C | |
| ENST00000256785.5:c.892A>C MANE Select | ENSP00000256785.4:p.Arg298= | |
| ENST00000256785.4:c.892A>C | ENSP00000256785.4:p.Arg298= | |
| NM_030787.3:c.892A>C , LRG_227t1:c.892A>C | NP_110414.1:p.Arg298= | |
| XM_011510020.1:c.901A>C | XP_011508322.1:p.Arg301= | |
| XM_011510020.2:c.901A>C | XP_011508322.1:p.Arg301= | |
| NM_030787.4:c.892A>C MANE Select | NP_110414.1:p.Arg298= |