Linked Data
MyVariant Identifiers:
chr20:g.23028729G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.23048092G>C , CM000682.2:g.23048092G>C | GRCh38 |
| NC_000020.10:g.23028729G>C , CM000682.1:g.23028729G>C | GRCh37 |
| NC_000020.9:g.22976729G>C | NCBI36 |
| NG_012027.1:g.6573C>G , LRG_168:g.6573C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000377103.3:c.1413C>G MANE Select | ENSP00000366307.2:p.Ala471= | |
| ENST00000377103.2:c.1413C>G | ENSP00000366307.2:p.Ala471= | |
| NM_000361.2:c.1413C>G , LRG_168t1:c.1413C>G | NP_000352.1:p.Ala471= | |
| NM_000361.3:c.1413C>G MANE Select | NP_000352.1:p.Ala471= |