Linked Data
ClinVar Variation Id:
1670418
ClinVar RCV Id:
RCV002203709
dbSNP Id:
rs2146818913
MyVariant Identifiers:
chr19:g.36332624G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.35841722G>A , CM000681.2:g.35841722G>A | GRCh38 |
| NC_000019.9:g.36332624G>A , CM000681.1:g.36332624G>A | GRCh37 |
| NC_000019.8:g.41024464G>A | NCBI36 |
| NG_013356.2:g.32566C>T , LRG_693:g.32566C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378910.10:c.2808C>T MANE Select | ENSP00000368190.4:p.Val936= | |
| ENST00000353632.6:c.2808C>T | ENSP00000343634.5:p.Val936= | |
| ENST00000378910.9:c.2808C>T | ENSP00000368190.4:p.Val936= | |
| NM_004646.3:c.2808C>T , LRG_693t1:c.2808C>T | NP_004637.1:p.Val936= | |
| NM_004646.4:c.2808C>T MANE Select | NP_004637.1:p.Val936= |