Linked Data
MyVariant Identifiers:
chr10:g.89487162A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.87727405A>T , CM000672.2:g.87727405A>T | GRCh38 |
| NC_000010.10:g.89487162A>T , CM000672.1:g.89487162A>T | GRCh37 |
| NC_000010.9:g.89477142A>T | NCBI36 |
| NG_012150.1:g.72687A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000456849.2:c.1002A>T MANE Select | ENSP00000406157.1:p.Arg334= | |
| ENST00000361175.8:c.987A>T | ENSP00000354436.4:p.Arg329= | |
| ENST00000456849.1:c.1002A>T | ENSP00000406157.1:p.Arg334= | |
| NM_001015880.1:c.1002A>T | NP_001015880.1:p.Arg334= | |
| NM_004670.3:c.987A>T | NP_004661.2:p.Arg329= | |
| NM_001015880.2:c.1002A>T MANE Select | NP_001015880.1:p.Arg334= | |
| NM_004670.4:c.987A>T | NP_004661.2:p.Arg329= |