Linked Data
MyVariant Identifiers:
chr19:g.18499694G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.18388884G>C , CM000681.2:g.18388884G>C | GRCh38 |
| NC_000019.9:g.18499694G>C , CM000681.1:g.18499694G>C | GRCh37 |
| NC_000019.8:g.18360694G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000595973.3:c.876G>C | ENSP00000470531.3:p.Val292= | |
| ENST00000597765.2:c.876G>C | ENSP00000469819.2:p.Val292= | |
| ENST00000252809.3:c.876G>C MANE Select | ENSP00000252809.3:p.Val292= | |
| NM_004864.2:c.876G>C | NP_004855.2:p.Val292= | |
| NM_004864.3:c.876G>C | NP_004855.2:p.Val292= | |
| XM_024451789.1:c.876G>C | XP_024307557.1:p.Val292= | |
| NM_004864.4:c.876G>C MANE Select | NP_004855.2:p.Val292= |