Linked Data
MyVariant Identifiers:
chr17:g.72916076A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.74919981A>G , CM000679.2:g.74919981A>G | GRCh38 |
| NC_000017.10:g.72916076A>G , CM000679.1:g.72916076A>G | GRCh37 |
| NC_000017.9:g.70427671A>G | NCBI36 |
| NG_007882.1:g.8276T>C | |
| NG_033062.1:g.707A>G | |
| NG_007882.2:g.8283T>C | |
| NG_033062.2:g.707A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000614341.5:c.855T>C MANE Select | ENSP00000480279.1:p.Arg285= | |
| ENST00000579243.1:c.*454T>C | ENSP00000462568.1:n.*454T>C | |
| ENST00000614341.4:c.855T>C | ENSP00000480279.1:p.Arg285= | |
| NM_001282489.2:c.546T>C | NP_001269418.1:p.Arg182= | |
| NM_173477.4:c.855T>C | NP_775748.2:p.Arg285= | |
| XM_011524296.1:c.546T>C | XP_011522598.1:p.Arg182= | |
| XM_011524296.2:c.546T>C | XP_011522598.1:p.Arg182= | |
| NM_173477.5:c.855T>C MANE Select | NP_775748.2:p.Arg285= | |
| NM_001282489.3:c.546T>C | NP_001269418.1:p.Arg182= |