Linked Data
MyVariant Identifiers:
chr1:g.59042382C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.58576710C>A , CM000663.2:g.58576710C>A | GRCh38 |
| NC_000001.10:g.59042382C>A , CM000663.1:g.59042382C>A | GRCh37 |
| NC_000001.9:g.58814970C>A | NCBI36 |
| NG_016237.1:g.5785G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371225.4:c.447G>T MANE Select | ENSP00000360269.2:p.Val149= | |
| ENST00000371225.3:c.447G>T | ENSP00000360269.2:p.Val149= | |
| NM_002353.2:c.447G>T | NP_002344.2:p.Val149= | |
| NM_002353.3:c.447G>T MANE Select | NP_002344.2:p.Val149= |