Linked Data
MyVariant Identifiers:
chr10:g.48389192G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.47350170C>T , CM000672.2:g.47350170C>T | GRCh38 |
| NC_000010.10:g.48389192G>A , CM000672.1:g.48389192G>A | GRCh37 |
| NC_000010.9:g.48009198G>A | NCBI36 |
| NG_029718.1:g.6800C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000584701.2:c.1686C>T MANE Select | ENSP00000463151.1:p.Ala562= | |
| ENST00000584701.1:c.1686C>T | ENSP00000463151.1:p.Ala562= | |
| NM_002900.2:c.1686C>T | NP_002891.1:p.Ala562= | |
| NM_002900.3:c.1686C>T MANE Select | NP_002891.1:p.Ala562= |