Linked Data
MyVariant Identifiers:
chr3:g.119133038T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.119414191T>G , CM000665.2:g.119414191T>G | GRCh38 |
| NC_000003.11:g.119133038T>G , CM000665.1:g.119133038T>G | GRCh37 |
| NC_000003.10:g.120615728T>G | NCBI36 |
| NG_007665.2:g.124819T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264245.9:c.2262T>G MANE Select | ENSP00000264245.4:p.Pro754= | |
| ENST00000264245.8:c.2262T>G | ENSP00000264245.4:p.Pro754= | |
| NM_020754.3:c.2262T>G | NP_065805.2:p.Pro754= | |
| XM_005247671.3:c.2169T>G | XP_005247728.1:p.Pro723= | |
| XM_006713714.2:c.2202T>G | XP_006713777.1:p.Pro734= | |
| XM_006713714.3:c.2202T>G | XP_006713777.1:p.Pro734= | |
| XM_017006955.1:c.1770T>G | XP_016862444.1:p.Pro590= | |
| NM_020754.4:c.2262T>G MANE Select | NP_065805.2:p.Pro754= |