Linked Data
MyVariant Identifiers:
chr15:g.74632041C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.74339700C>T , CM000677.2:g.74339700C>T | GRCh38 |
| NC_000015.9:g.74632041C>T , CM000677.1:g.74632041C>T | GRCh37 |
| NC_000015.8:g.72419094C>T | NCBI36 |
| NG_007973.1:g.33042G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000268053.11:c.1044G>A MANE Select | ENSP00000268053.6:p.Val348= | |
| ENST00000268053.10:c.1044G>A | ENSP00000268053.6:p.Val348= | |
| ENST00000358632.8:c.570G>A | ENSP00000351455.4:p.Val190= | |
| ENST00000435365.5:c.1044G>A | ENSP00000391081.1:p.Val348= | |
| ENST00000566674.5:c.570G>A | ENSP00000456941.1:p.Val190= | |
| NM_000781.2:c.1044G>A | NP_000772.2:p.Val348= | |
| NM_001099773.1:c.570G>A | NP_001093243.1:p.Val190= | |
| NM_000781.3:c.1044G>A MANE Select | NP_000772.2:p.Val348= | |
| NM_001099773.2:c.570G>A | NP_001093243.1:p.Val190= |