Linked Data
MyVariant Identifiers:
chr10:g.17849708T>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.17849708T>C , CM000672.2:g.17849708T>C | GRCh38 |
| NG_047011.1:g.45366T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000569591.3:c.1193T>C MANE Select | ENSP00000455897.1:p.Leu398Pro | |
| ENST00000569591.2:c.1193T>C | ENSP00000455897.1:p.Leu398Pro | |
| NM_002438.3:c.1193T>C | NP_002429.1:p.Leu398Pro | |
| NM_002438.4:c.1193T>C MANE Select | NP_002429.1:p.Leu398Pro |