Linked Data
MyVariant Identifiers:
chr7:g.17379315A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.17339691A>G , CM000669.2:g.17339691A>G | GRCh38 |
| NC_000007.13:g.17379315A>G , CM000669.1:g.17379315A>G | GRCh37 |
| NC_000007.12:g.17345840A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000242057.9:c.1866A>G MANE Select | ENSP00000242057.4:p.Gln622= | |
| ENST00000637807.1:c.1836A>G | ENSP00000490530.1:p.Gln612= | |
| ENST00000642825.1:c.1821A>G | ENSP00000495987.1:p.Gln607= | |
| ENST00000242057.8:c.1866A>G | ENSP00000242057.4:p.Gln622= | |
| ENST00000463496.1:c.1866A>G | ENSP00000436466.1:p.Gln622= | |
| NM_001621.4:c.1866A>G | NP_001612.1:p.Gln622= | |
| NM_001621.5:c.1866A>G MANE Select | NP_001612.1:p.Gln622= |