Linked Data
MyVariant Identifiers:
chr19:g.6714023C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6714012C>T , CM000681.2:g.6714012C>T | GRCh38 |
| NC_000019.9:g.6714023C>T , CM000681.1:g.6714023C>T | GRCh37 |
| NC_000019.8:g.6665023C>T | NCBI36 |
| NG_009557.1:g.11640G>A , LRG_27:g.11640G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695652.1:c.630G>A | ENSP00000512083.1:p.Leu210= | |
| ENST00000245907.11:c.753G>A MANE Select | ENSP00000245907.4:p.Leu251= | |
| ENST00000245907.10:c.753G>A | ENSP00000245907.4:p.Leu251= | |
| ENST00000595577.1:n.257G>A | ||
| NM_000064.3:c.753G>A | NP_000055.2:p.Leu251= | |
| NM_000064.4:c.753G>A MANE Select | NP_000055.2:p.Leu251= |