Linked Data
ClinVar Variation Id:
2944199
ClinVar RCV Id:
RCV003805949
MyVariant Identifiers:
chr10:g.121431961A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.119672449A>G , CM000672.2:g.119672449A>G | GRCh38 |
| NC_000010.10:g.121431961A>G , CM000672.1:g.121431961A>G | GRCh37 |
| NC_000010.9:g.121421951A>G | NCBI36 |
| NG_016125.1:g.26080A>G , LRG_742:g.26080A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369085.8:c.702A>G MANE Select | ENSP00000358081.4:p.Pro234= | |
| ENST00000369085.7:c.702A>G | ENSP00000358081.3:p.Pro234= | |
| ENST00000450186.1:c.528A>G | ENSP00000410036.1:p.Pro176= | |
| NM_004281.3:c.702A>G , LRG_742t1:c.702A>G | NP_004272.2:p.Pro234= | |
| XM_005270287.1:c.702A>G | XP_005270344.1:p.Pro234= | |
| XM_005270287.2:c.702A>G | XP_005270344.1:p.Pro234= | |
| NM_004281.4:c.702A>G MANE Select | NP_004272.2:p.Pro234= |