Linked Data
gnomAD v4:
2-219060358-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.219060358C>T , CM000664.2:g.219060358C>T | GRCh38 |
| NC_000002.11:g.219925080C>T , CM000664.1:g.219925080C>T | GRCh37 |
| NC_000002.10:g.219633324C>T | NCBI36 |
| NG_016741.1:g.5159G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000295731.7:c.110G>A MANE Select | ENSP00000295731.5:p.Arg37His | |
| ENST00000295731.6:c.110G>A | ENSP00000295731.5:p.Arg37His | |
| NM_002181.3:c.110G>A | NP_002172.2:p.Arg37His | |
| NM_002181.4:c.110G>A MANE Select | NP_002172.2:p.Arg37His |