Linked Data
gnomAD v4:
2-218882171-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.218882171A>G , CM000664.2:g.218882171A>G | GRCh38 |
| NC_000002.11:g.219746893A>G , CM000664.1:g.219746893A>G | GRCh37 |
| NC_000002.10:g.219455137A>G | NCBI36 |
| NG_012179.1:g.6639A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258411.8:c.124A>G MANE Select | ENSP00000258411.3:p.Asn42Asp | |
| ENST00000258411.7:c.124A>G | ENSP00000258411.3:p.Asn42Asp | |
| ENST00000458582.1:c.11A>G | ||
| NM_025216.2:c.124A>G | NP_079492.2:p.Asn42Asp | |
| XM_011511928.1:c.73A>G | XP_011510230.1:p.Asn25Asp | |
| XM_011511929.1:c.28A>G | XP_011510231.1:p.Asn10Asp | |
| XM_011511930.1:c.124A>G | XP_011510232.1:p.Asn42Asp | |
| XM_011511929.2:c.28A>G | XP_011510231.1:p.Asn10Asp | |
| NM_025216.3:c.124A>G MANE Select | NP_079492.2:p.Asn42Asp |