Linked Data
ClinVar Variation Id:
2945366
ClinVar RCV Id:
RCV003801020
MyVariant Identifiers:
chr14:g.21780621A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.21312462A>G , CM000676.2:g.21312462A>G | GRCh38 |
| NC_000014.8:g.21780621A>G , CM000676.1:g.21780621A>G | GRCh37 |
| NC_000014.7:g.20850461A>G | NCBI36 |
| NG_008933.1:g.29486A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000400017.7:c.1107A>G MANE Select | ENSP00000382895.2:p.Lys369= | |
| ENST00000400017.6:c.1107A>G | ENSP00000382895.2:p.Lys369= | |
| ENST00000556336.5:c.1026A>G | ENSP00000450445.1:p.Lys342= | |
| ENST00000557771.5:c.1026A>G | ENSP00000451219.1:p.Lys342= | |
| NM_020366.3:c.1107A>G | NP_065099.3:p.Lys369= | |
| XM_011536983.1:c.1074A>G | XP_011535285.1:p.Lys358= | |
| NM_020366.4:c.1107A>G MANE Select | NP_065099.3:p.Lys369= |