Linked Data
MyVariant Identifiers:
chr7:g.152345799T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.152648714T>A , CM000669.2:g.152648714T>A | GRCh38 |
| NC_000007.13:g.152345799T>A , CM000669.1:g.152345799T>A | GRCh37 |
| NC_000007.12:g.151976732T>A | NCBI36 |
| NG_027988.1:g.32452A>T | |
| NG_027988.2:g.32452A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000698506.1:c.603A>T | ENSP00000513758.1:p.Ser201= | |
| ENST00000359321.2:c.771A>T MANE Select | ENSP00000352271.1:p.Ser257= | |
| ENST00000359321.1:c.771A>T | ENSP00000352271.1:p.Ser257= | |
| ENST00000495707.1:n.793A>T | ||
| NM_005431.1:c.771A>T | NP_005422.1:p.Ser257= | |
| NM_005431.2:c.771A>T MANE Select | NP_005422.1:p.Ser257= |