Linked Data
MyVariant Identifiers:
chr19:g.36340008G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.35849106G>C , CM000681.2:g.35849106G>C | GRCh38 |
| NC_000019.9:g.36340008G>C , CM000681.1:g.36340008G>C | GRCh37 |
| NC_000019.8:g.41031848G>C | NCBI36 |
| NG_013356.2:g.25182C>G , LRG_693:g.25182C>G | |
| NG_051206.1:g.2472G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378910.10:c.882C>G MANE Select | ENSP00000368190.4:p.Thr294= | |
| ENST00000353632.6:c.882C>G | ENSP00000343634.5:p.Thr294= | |
| ENST00000378910.9:c.882C>G | ENSP00000368190.4:p.Thr294= | |
| NM_004646.3:c.882C>G , LRG_693t1:c.882C>G | NP_004637.1:p.Thr294= | |
| NM_004646.4:c.882C>G MANE Select | NP_004637.1:p.Thr294= |