Linked Data
gnomAD v4:
3-42688223-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.42688223A>G , CM000665.2:g.42688223A>G | GRCh38 |
| NC_000003.11:g.42729715A>G , CM000665.1:g.42729715A>G | GRCh37 |
| NC_000003.10:g.42704719A>G | NCBI36 |
| NG_033035.1:g.7705A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000287777.5:c.1234A>G MANE Select | ENSP00000287777.4:p.Asn412Asp | |
| ENST00000287777.4:c.1234A>G | ENSP00000287777.4:p.Asn412Asp | |
| NM_152393.3:c.1234A>G | NP_689606.2:p.Asn412Asp | |
| XM_005264866.2:c.1234A>G | XP_005264923.1:p.Asn412Asp | |
| NM_152393.4:c.1234A>G MANE Select | NP_689606.2:p.Asn412Asp |