Linked Data
MyVariant Identifiers:
chr2:g.219925079G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.219060357G>C , CM000664.2:g.219060357G>C | GRCh38 |
| NC_000002.11:g.219925079G>C , CM000664.1:g.219925079G>C | GRCh37 |
| NC_000002.10:g.219633323G>C | NCBI36 |
| NG_016741.1:g.5160C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000295731.7:c.111C>G MANE Select | ENSP00000295731.5:p.Arg37= | |
| ENST00000295731.6:c.111C>G | ENSP00000295731.5:p.Arg37= | |
| NM_002181.3:c.111C>G | NP_002172.2:p.Arg37= | |
| NM_002181.4:c.111C>G MANE Select | NP_002172.2:p.Arg37= |