Linked Data
MyVariant Identifiers:
chr10:g.112540835T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.110781077T>G , CM000672.2:g.110781077T>G | GRCh38 |
| NC_000010.10:g.112540835T>G , CM000672.1:g.112540835T>G | GRCh37 |
| NC_000010.9:g.112530825T>G | NCBI36 |
| NG_021177.1:g.141681T>G , LRG_382:g.141681T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369519.4:c.468T>G MANE Select | ENSP00000358532.3:p.Ala156= | |
| ENST00000369519.3:c.468T>G | ENSP00000358532.3:p.Ala156= | |
| NM_001134363.2:c.468T>G | NP_001127835.2:p.Ala156= | |
| XM_011539697.1:c.84T>G | XP_011537999.1:p.Ala28= | |
| XM_017016103.2:c.303T>G | XP_016871592.1:p.Ala101= | |
| XM_017016104.2:c.84T>G | XP_016871593.1:p.Ala28= | |
| NM_001134363.3:c.468T>G MANE Select | NP_001127835.2:p.Ala156= |