Linked Data
MyVariant Identifiers:
chr19:g.6709821C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6709810C>T , CM000681.2:g.6709810C>T | GRCh38 |
| NC_000019.9:g.6709821C>T , CM000681.1:g.6709821C>T | GRCh37 |
| NC_000019.8:g.6660821C>T | NCBI36 |
| NG_009557.1:g.15842G>A , LRG_27:g.15842G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695652.1:c.1596G>A | ENSP00000512083.1:p.Arg532= | |
| ENST00000695654.1:c.843G>A | ENSP00000512085.1:p.Arg281= | |
| ENST00000695655.1:c.660G>A | ENSP00000512086.1:n.660G>A | |
| ENST00000695692.1:n.1083G>A | ||
| ENST00000245907.11:c.1719G>A MANE Select | ENSP00000245907.4:p.Arg573= | |
| ENST00000245907.10:c.1719G>A | ENSP00000245907.4:p.Arg573= | |
| ENST00000600763.1:n.352G>A | ||
| NM_000064.3:c.1719G>A | NP_000055.2:p.Arg573= | |
| NM_000064.4:c.1719G>A MANE Select | NP_000055.2:p.Arg573= |