Linked Data
dbSNP Id:
rs1313648676
gnomAD v2:
3-119132970-A-G
gnomAD v3:
3-119414123-A-G
gnomAD v4:
3-119414123-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.119414123A>G , CM000665.2:g.119414123A>G | GRCh38 |
| NC_000003.11:g.119132970A>G , CM000665.1:g.119132970A>G | GRCh37 |
| NC_000003.10:g.120615660A>G | NCBI36 |
| NG_007665.2:g.124751A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264245.9:c.2194A>G MANE Select | ENSP00000264245.4:p.Thr732Ala | |
| ENST00000264245.8:c.2194A>G | ENSP00000264245.4:p.Thr732Ala | |
| NM_020754.3:c.2194A>G | NP_065805.2:p.Thr732Ala | |
| XM_005247671.3:c.2101A>G | XP_005247728.1:p.Thr701Ala | |
| XM_006713714.2:c.2134A>G | XP_006713777.1:p.Thr712Ala | |
| XM_006713714.3:c.2134A>G | XP_006713777.1:p.Thr712Ala | |
| XM_017006955.1:c.1702A>G | XP_016862444.1:p.Thr568Ala | |
| NM_020754.4:c.2194A>G MANE Select | NP_065805.2:p.Thr732Ala |