Linked Data
MyVariant Identifiers:
chr7:g.152373146T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.152676061T>G , CM000669.2:g.152676061T>G | GRCh38 |
| NC_000007.13:g.152373146T>G , CM000669.1:g.152373146T>G | GRCh37 |
| NC_000007.12:g.152004079T>G | NCBI36 |
| NG_027988.1:g.5105A>C | |
| NG_027988.2:g.5105A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000698506.1:c.-68A>C | ENSP00000513758.1:n.-68A>C | |
| ENST00000698507.1:n.87A>C | ||
| ENST00000359321.2:c.19A>C MANE Select | ENSP00000352271.1:p.Arg7= | |
| ENST00000359321.1:c.19A>C | ENSP00000352271.1:p.Arg7= | |
| NM_005431.1:c.19A>C | NP_005422.1:p.Arg7= | |
| NM_005431.2:c.19A>C MANE Select | NP_005422.1:p.Arg7= |