Linked Data
ClinVar Variation Id:
2586448
ClinVar RCV Id:
RCV003358325
MyVariant Identifiers:
chr20:g.42744365G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.44115725G>T , CM000682.2:g.44115725G>T | GRCh38 |
| NC_000020.10:g.42744365G>T , CM000682.1:g.42744365G>T | GRCh37 |
| NC_000020.9:g.42177779G>T | NCBI36 |
| NG_031867.1:g.76854C>A , LRG_394:g.76854C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372980.4:c.1950C>A MANE Select | ENSP00000362071.3:p.Ala650= | |
| ENST00000372980.3:c.1950C>A | ENSP00000362071.3:p.Ala650= | |
| NM_020433.4:c.1950C>A , LRG_394t1:c.1950C>A | NP_065166.2:p.Ala650= | |
| XM_006723832.2:c.1950C>A | XP_006723895.1:p.Ala650= | |
| NM_020433.5:c.1950C>A MANE Select | NP_065166.2:p.Ala650= |