Linked Data
MyVariant Identifiers:
chr2:g.219925088C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.219060366C>T , CM000664.2:g.219060366C>T | GRCh38 |
| NC_000002.11:g.219925088C>T , CM000664.1:g.219925088C>T | GRCh37 |
| NC_000002.10:g.219633332C>T | NCBI36 |
| NG_016741.1:g.5151G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000295731.7:c.102G>A MANE Select | ENSP00000295731.5:p.Val34= | |
| ENST00000295731.6:c.102G>A | ENSP00000295731.5:p.Val34= | |
| NM_002181.3:c.102G>A | NP_002172.2:p.Val34= | |
| NM_002181.4:c.102G>A MANE Select | NP_002172.2:p.Val34= |