Linked Data
MyVariant Identifiers:
chr19:g.6713282C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6713271C>G , CM000681.2:g.6713271C>G | GRCh38 |
| NC_000019.9:g.6713282C>G , CM000681.1:g.6713282C>G | GRCh37 |
| NC_000019.8:g.6664282C>G | NCBI36 |
| NG_009557.1:g.12381G>C , LRG_27:g.12381G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695652.1:c.798G>C | ENSP00000512083.1:p.Leu266= | |
| ENST00000695654.1:c.45G>C | ENSP00000512085.1:p.Leu15= | |
| ENST00000695692.1:n.245G>C | ||
| ENST00000245907.11:c.921G>C MANE Select | ENSP00000245907.4:p.Leu307= | |
| ENST00000245907.10:c.921G>C | ENSP00000245907.4:p.Leu307= | |
| ENST00000594270.5:n.45G>C | ||
| ENST00000595577.1:n.425G>C | ||
| ENST00000597442.5:n.171G>C | ||
| NM_000064.3:c.921G>C | NP_000055.2:p.Leu307= | |
| NM_000064.4:c.921G>C MANE Select | NP_000055.2:p.Leu307= |