Linked Data
dbSNP Id:
rs1377614762
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.29226995G>C , CM000664.2:g.29226995G>C | GRCh38 |
| NC_000002.11:g.29449861G>C , CM000664.1:g.29449861G>C | GRCh37 |
| NC_000002.10:g.29303365G>C | NCBI36 |
| NG_009445.1:g.699572C>G , LRG_488:g.699572C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000389048.8:c.2994C>G MANE Select | ENSP00000373700.3:p.Asp998Glu | |
| ENST00000431873.6:c.160C>G | ||
| ENST00000389048.7:c.2994C>G | ENSP00000373700.3:p.Asp998Glu | |
| ENST00000618119.4:c.1863C>G | ENSP00000482733.1:p.Asp621Glu | |
| NM_004304.4:c.2994C>G | NP_004295.2:p.Asp998Glu | |
| XM_024452778.1:c.147C>G | XP_024308546.1:p.Asp49Glu | |
| XR_001738688.2:n.3850C>G | ||
| NM_004304.5:c.2994C>G MANE Select | NP_004295.2:p.Asp998Glu |