Linked Data
MyVariant Identifiers:
chr7:g.152345913C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.152648828C>T , CM000669.2:g.152648828C>T | GRCh38 |
| NC_000007.13:g.152345913C>T , CM000669.1:g.152345913C>T | GRCh37 |
| NC_000007.12:g.151976846C>T | NCBI36 |
| NG_027988.1:g.32338G>A | |
| NG_027988.2:g.32338G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000698506.1:c.489G>A | ENSP00000513758.1:p.Val163= | |
| ENST00000359321.2:c.657G>A MANE Select | ENSP00000352271.1:p.Val219= | |
| ENST00000359321.1:c.657G>A | ENSP00000352271.1:p.Val219= | |
| ENST00000495707.1:n.679G>A | ||
| NM_005431.1:c.657G>A | NP_005422.1:p.Val219= | |
| NM_005431.2:c.657G>A MANE Select | NP_005422.1:p.Val219= |