Linked Data
MyVariant Identifiers:
chr20:g.2398123A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.2417477A>C , CM000682.2:g.2417477A>C | GRCh38 |
| NC_000020.10:g.2398123A>C , CM000682.1:g.2398123A>C | GRCh37 |
| NC_000020.9:g.2346123A>C | NCBI36 |
| NG_031917.1:g.41570A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000202625.7:c.1582A>C MANE Select | ENSP00000202625.2:p.Arg528= | |
| ENST00000202625.6:c.1582A>C | ENSP00000202625.2:p.Arg528= | |
| ENST00000381423.1:c.1582A>C | ENSP00000370831.1:p.Arg528= | |
| NM_001254734.1:c.1582A>C | NP_001241663.1:p.Arg528= | |
| NM_198994.2:c.1582A>C | NP_945345.2:p.Arg528= | |
| NM_001254734.2:c.1582A>C | NP_001241663.1:p.Arg528= | |
| NM_198994.3:c.1582A>C MANE Select | NP_945345.2:p.Arg528= |