Linked Data
ClinVar Variation Id:
1748108
ClinVar RCV Id:
RCV002351798
MyVariant Identifiers:
chr7:g.152346018T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.152648933T>G , CM000669.2:g.152648933T>G | GRCh38 |
| NC_000007.13:g.152346018T>G , CM000669.1:g.152346018T>G | GRCh37 |
| NC_000007.12:g.151976951T>G | NCBI36 |
| NG_027988.1:g.32233A>C | |
| NG_027988.2:g.32233A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000698506.1:c.384A>C | ENSP00000513758.1:p.Val128= | |
| ENST00000359321.2:c.552A>C MANE Select | ENSP00000352271.1:p.Val184= | |
| ENST00000359321.1:c.552A>C | ENSP00000352271.1:p.Val184= | |
| ENST00000495707.1:n.574A>C | ||
| NM_005431.1:c.552A>C | NP_005422.1:p.Val184= | |
| NM_005431.2:c.552A>C MANE Select | NP_005422.1:p.Val184= |