Linked Data
MyVariant Identifiers:
chr10:g.112540826C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.110781068C>A , CM000672.2:g.110781068C>A | GRCh38 |
| NC_000010.10:g.112540826C>A , CM000672.1:g.112540826C>A | GRCh37 |
| NC_000010.9:g.112530816C>A | NCBI36 |
| NG_021177.1:g.141672C>A , LRG_382:g.141672C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000369519.4:c.459C>A MANE Select | ENSP00000358532.3:p.Pro153= | |
| ENST00000369519.3:c.459C>A | ENSP00000358532.3:p.Pro153= | |
| NM_001134363.2:c.459C>A | NP_001127835.2:p.Pro153= | |
| XM_011539697.1:c.75C>A | XP_011537999.1:p.Pro25= | |
| XM_017016103.2:c.294C>A | XP_016871592.1:p.Pro98= | |
| XM_017016104.2:c.75C>A | XP_016871593.1:p.Pro25= | |
| NM_001134363.3:c.459C>A MANE Select | NP_001127835.2:p.Pro153= |