Linked Data
MyVariant Identifiers:
chr19:g.6714368G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6714357G>C , CM000681.2:g.6714357G>C | GRCh38 |
| NC_000019.9:g.6714368G>C , CM000681.1:g.6714368G>C | GRCh37 |
| NC_000019.8:g.6665368G>C | NCBI36 |
| NG_009557.1:g.11295C>G , LRG_27:g.11295C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695652.1:c.471C>G | ENSP00000512083.1:p.Leu157= | |
| ENST00000245907.11:c.594C>G MANE Select | ENSP00000245907.4:p.Leu198= | |
| ENST00000245907.10:c.594C>G | ENSP00000245907.4:p.Leu198= | |
| NM_000064.3:c.594C>G | NP_000055.2:p.Leu198= | |
| NM_000064.4:c.594C>G MANE Select | NP_000055.2:p.Leu198= |