Linked Data
MyVariant Identifiers:
chr7:g.152345766A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.152648681A>G , CM000669.2:g.152648681A>G | GRCh38 |
| NC_000007.13:g.152345766A>G , CM000669.1:g.152345766A>G | GRCh37 |
| NC_000007.12:g.151976699A>G | NCBI36 |
| NG_027988.1:g.32485T>C | |
| NG_027988.2:g.32485T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000698506.1:c.636T>C | ENSP00000513758.1:p.His212= | |
| ENST00000359321.2:c.804T>C MANE Select | ENSP00000352271.1:p.His268= | |
| ENST00000359321.1:c.804T>C | ENSP00000352271.1:p.His268= | |
| ENST00000495707.1:n.826T>C | ||
| NM_005431.1:c.804T>C | NP_005422.1:p.His268= | |
| NM_005431.2:c.804T>C MANE Select | NP_005422.1:p.His268= |