Linked Data
MyVariant Identifiers:
chr19:g.9237378C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.9126702C>G , CM000681.2:g.9126702C>G | GRCh38 |
| NC_000019.9:g.9237378C>G , CM000681.1:g.9237378C>G | GRCh37 |
| NC_000019.8:g.9098378C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000305444.2:c.249G>C MANE Select | ENSP00000302867.2:p.Val83= | |
| NM_001001958.1:c.249G>C MANE Select | NP_001001958.1:p.Val83= |