Linked Data
MyVariant Identifiers:
chr6:g.32188570C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32220793C>A , CM000668.2:g.32220793C>A | GRCh38 |
| NC_000006.11:g.32188570C>A , CM000668.1:g.32188570C>A | GRCh37 |
| NC_000006.10:g.32296548C>A | NCBI36 |
| NG_028190.1:g.8275G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375023.3:c.885G>T MANE Select | ENSP00000364163.3:p.Leu295= | |
| ENST00000473562.1:n.1014G>T | ||
| NM_004557.3:c.885G>T | NP_004548.3:p.Leu295= | |
| NR_134949.1:n.1024G>T | ||
| NR_134950.1:n.1024G>T | ||
| NM_004557.4:c.885G>T MANE Select | NP_004548.3:p.Leu295= | |
| NR_134949.2:n.1024G>T | ||
| NR_134950.2:n.1024G>T |