Linked Data
MyVariant Identifiers:
chr19:g.9237528G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.9126852G>A , CM000681.2:g.9126852G>A | GRCh38 |
| NC_000019.9:g.9237528G>A , CM000681.1:g.9237528G>A | GRCh37 |
| NC_000019.8:g.9098528G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000305444.2:c.99C>T MANE Select | ENSP00000302867.2:p.Ser33= | |
| NM_001001958.1:c.99C>T MANE Select | NP_001001958.1:p.Ser33= |