Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.3218695C>T , CM000673.2:g.3218695C>T | GRCh38 |
| NC_000011.9:g.3239925C>T , CM000673.1:g.3239925C>T | GRCh37 |
| NC_000011.8:g.3196501C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001164377.1:c.119G>A (MRGPRG) MANE Select | NP_001157849.1:p.Arg40His |
| ENST00000332314.3:c.119G>A (MRGPRG) MANE Select | ENSP00000330612.3:p.Arg40His |
| NR_027138.1:n.228+136C>T (MRGPRG-AS1) |