Linked Data
MyVariant Identifiers:
chr15:g.48796108A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48503911A>C , CM000677.2:g.48503911A>C | GRCh38 |
| NC_000015.9:g.48796108A>C , CM000677.1:g.48796108A>C | GRCh37 |
| NC_000015.8:g.46583400A>C | NCBI36 |
| NG_008805.2:g.146878T>G , LRG_778:g.146878T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559133.6:c.1989T>G | ENSP00000453958.2:p.Gly663= | |
| ENST00000674301.2:c.1989T>G | ENSP00000501333.2:p.Gly663= | |
| ENST00000684448.1:n.663T>G | ||
| ENST00000316623.10:c.1989T>G MANE Select | ENSP00000325527.5:p.Gly663= | |
| ENST00000316623.9:c.1989T>G | ENSP00000325527.5:p.Gly663= | |
| ENST00000537463.6:c.637-29261T>G | ENSP00000440294.2:n.637-29261T>G | |
| NM_000138.4:c.1989T>G , LRG_778t1:c.1989T>G | NP_000129.3:p.Gly663= | |
| NM_000138.5:c.1989T>G MANE Select | NP_000129.3:p.Gly663= |