Linked Data
dbSNP Id:
rs63750519
ExAC:
11:5247881 T / C
gnomAD v2:
11-5247881-T-C
gnomAD v3:
11-5226651-T-C
gnomAD v4:
11-5226651-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5226651T>C , CM000673.2:g.5226651T>C | GRCh38 |
| NC_000011.9:g.5247881T>C , CM000673.1:g.5247881T>C | GRCh37 |
| NC_000011.8:g.5204457T>C | NCBI36 |
| NG_000007.3:g.70965A>G | |
| NG_059281.1:g.5421A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647020.1:c.241A>G | ENSP00000494175.1:p.Asn81Asp | |
| ENST00000335295.4:c.241A>G MANE Select | ENSP00000333994.3:p.Asn81Asp | |
| ENST00000380315.2:c.241A>G | ENSP00000369671.2:p.Asn81Asp | |
| ENST00000475226.1:n.173A>G | ||
| ENST00000485743.1:n.292A>G | ||
| ENST00000633227.1:c.*57A>G | ENSP00000488004.1:n.*57A>G | |
| NM_000518.4:c.241A>G | NP_000509.1:p.Asn81Asp | |
| NM_000518.5:c.241A>G MANE Select | NP_000509.1:p.Asn81Asp |