Linked Data
MyVariant Identifiers:
chr19:g.36339692G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.35848790G>T , CM000681.2:g.35848790G>T | GRCh38 |
| NC_000019.9:g.36339692G>T , CM000681.1:g.36339692G>T | GRCh37 |
| NC_000019.8:g.41031532G>T | NCBI36 |
| NG_013356.2:g.25498C>A , LRG_693:g.25498C>A | |
| NG_051206.1:g.2156G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378910.10:c.1017C>A MANE Select | ENSP00000368190.4:p.Pro339= | |
| ENST00000353632.6:c.1017C>A | ENSP00000343634.5:p.Pro339= | |
| ENST00000378910.9:c.1017C>A | ENSP00000368190.4:p.Pro339= | |
| ENST00000592132.1:n.24C>A | ||
| NM_004646.3:c.1017C>A , LRG_693t1:c.1017C>A | NP_004637.1:p.Pro339= | |
| NM_004646.4:c.1017C>A MANE Select | NP_004637.1:p.Pro339= |