Linked Data
ClinVar Variation Id:
2027328
ClinVar RCV Id:
RCV002889442
MyVariant Identifiers:
chr8:g.19811683T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.19954172T>C , CM000670.2:g.19954172T>C | GRCh38 |
| NC_000008.10:g.19811683T>C , CM000670.1:g.19811683T>C | GRCh37 |
| NC_000008.9:g.19855963T>C | NCBI36 |
| NG_008855.1:g.20102T>C | |
| NG_008855.2:g.57456T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000650287.1:c.594T>C MANE Select | ENSP00000497642.1:p.Leu198= | |
| ENST00000311322.8:c.594T>C | ENSP00000309757.6:p.Leu198= | |
| NM_000237.2:c.594T>C | NP_000228.1:p.Leu198= | |
| NM_000237.3:c.594T>C MANE Select | NP_000228.1:p.Leu198= |