Linked Data
MyVariant Identifiers:
chr7:g.17379333G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.17339709G>A , CM000669.2:g.17339709G>A | GRCh38 |
| NC_000007.13:g.17379333G>A , CM000669.1:g.17379333G>A | GRCh37 |
| NC_000007.12:g.17345858G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000242057.9:c.1884G>A MANE Select | ENSP00000242057.4:p.Lys628= | |
| ENST00000637807.1:c.1854G>A | ENSP00000490530.1:p.Lys618= | |
| ENST00000642825.1:c.1839G>A | ENSP00000495987.1:p.Lys613= | |
| ENST00000242057.8:c.1884G>A | ENSP00000242057.4:p.Lys628= | |
| ENST00000463496.1:c.1884G>A | ENSP00000436466.1:p.Lys628= | |
| NM_001621.4:c.1884G>A | NP_001612.1:p.Lys628= | |
| NM_001621.5:c.1884G>A MANE Select | NP_001612.1:p.Lys628= |