Linked Data
MyVariant Identifiers:
chr19:g.6714386A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6714375A>T , CM000681.2:g.6714375A>T | GRCh38 |
| NC_000019.9:g.6714386A>T , CM000681.1:g.6714386A>T | GRCh37 |
| NC_000019.8:g.6665386A>T | NCBI36 |
| NG_009557.1:g.11277T>A , LRG_27:g.11277T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695652.1:c.453T>A | ENSP00000512083.1:p.Ser151= | |
| ENST00000245907.11:c.576T>A MANE Select | ENSP00000245907.4:p.Ser192= | |
| ENST00000245907.10:c.576T>A | ENSP00000245907.4:p.Ser192= | |
| NM_000064.3:c.576T>A | NP_000055.2:p.Ser192= | |
| NM_000064.4:c.576T>A MANE Select | NP_000055.2:p.Ser192= |