Linked Data
MyVariant Identifiers:
chr3:g.119133113T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.119414266T>G , CM000665.2:g.119414266T>G | GRCh38 |
| NC_000003.11:g.119133113T>G , CM000665.1:g.119133113T>G | GRCh37 |
| NC_000003.10:g.120615803T>G | NCBI36 |
| NG_007665.2:g.124894T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264245.9:c.2337T>G MANE Select | ENSP00000264245.4:p.Pro779= | |
| ENST00000264245.8:c.2337T>G | ENSP00000264245.4:p.Pro779= | |
| NM_020754.3:c.2337T>G | NP_065805.2:p.Pro779= | |
| XM_005247671.3:c.2244T>G | XP_005247728.1:p.Pro748= | |
| XM_006713714.2:c.2277T>G | XP_006713777.1:p.Pro759= | |
| XM_006713714.3:c.2277T>G | XP_006713777.1:p.Pro759= | |
| XM_017006955.1:c.1845T>G | XP_016862444.1:p.Pro615= | |
| NM_020754.4:c.2337T>G MANE Select | NP_065805.2:p.Pro779= |