Linked Data
MyVariant Identifiers:
chr20:g.6758936A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.6778289A>C , CM000682.2:g.6778289A>C | GRCh38 |
| NC_000020.10:g.6758936A>C , CM000682.1:g.6758936A>C | GRCh37 |
| NC_000020.9:g.6706936A>C | NCBI36 |
| NG_023233.1:g.15192A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378827.5:c.391A>C MANE Select | ENSP00000368104.3:p.Arg131= | |
| ENST00000378827.4:c.391A>C | ENSP00000368104.3:p.Arg131= | |
| NM_001200.2:c.391A>C | NP_001191.1:p.Arg131= | |
| XM_011529323.1:c.-78A>C | XP_011527625.1:n.-78A>C | |
| NM_001200.3:c.391A>C | NP_001191.1:p.Arg131= | |
| NM_001200.4:c.391A>C MANE Select | NP_001191.1:p.Arg131= |