Linked Data
dbSNP Id:
rs2148178419
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.29226963T>C , CM000664.2:g.29226963T>C | GRCh38 |
| NC_000002.11:g.29449829T>C , CM000664.1:g.29449829T>C | GRCh37 |
| NC_000002.10:g.29303333T>C | NCBI36 |
| NG_009445.1:g.699604A>G , LRG_488:g.699604A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000389048.8:c.3026A>G MANE Select | ENSP00000373700.3:p.Asp1009Gly | |
| ENST00000431873.6:c.192A>G | ||
| ENST00000389048.7:c.3026A>G | ENSP00000373700.3:p.Asp1009Gly | |
| ENST00000618119.4:c.1895A>G | ENSP00000482733.1:p.Asp632Gly | |
| NM_004304.4:c.3026A>G | NP_004295.2:p.Asp1009Gly | |
| XM_024452778.1:c.179A>G | XP_024308546.1:p.Asp60Gly | |
| XR_001738688.2:n.3882A>G | ||
| NM_004304.5:c.3026A>G MANE Select | NP_004295.2:p.Asp1009Gly |