Linked Data
MyVariant Identifiers:
chr5:g.110454765T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.111119067T>G , CM000667.2:g.111119067T>G | GRCh38 |
| NC_000005.9:g.110454765T>G , CM000667.1:g.110454765T>G | GRCh37 |
| NC_000005.8:g.110482664T>G | NCBI36 |
| NG_008979.1:g.31896T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000513710.4:c.1851T>G MANE Select | ENSP00000424628.3:p.Pro617= | |
| ENST00000506538.6:c.2019T>G | ENSP00000423067.2:p.Pro673= | |
| ENST00000513710.3:c.1851T>G | ENSP00000424628.3:p.Pro617= | |
| ENST00000612402.4:c.2019T>G | ENSP00000479950.1:p.Pro673= | |
| NM_139281.2:c.2019T>G | NP_644810.1:p.Pro673= | |
| XM_011543163.1:c.2019T>G | XP_011541465.1:p.Pro673= | |
| NM_139281.3:c.1851T>G MANE Select | NP_644810.2:p.Pro617= |