Linked Data
MyVariant Identifiers:
chr1:g.204128655C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.204159527C>T , CM000663.2:g.204159527C>T | GRCh38 |
| NC_000001.10:g.204128655C>T , CM000663.1:g.204128655C>T | GRCh37 |
| NC_000001.9:g.202395278C>T | NCBI36 |
| NG_012122.1:g.11811G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000272190.9:c.561G>A MANE Select | ENSP00000272190.8:p.Leu187= | |
| ENST00000638118.1:c.447G>A | ENSP00000490307.1:p.Leu149= | |
| ENST00000272190.8:c.561G>A | ENSP00000272190.8:p.Leu187= | |
| NM_000537.3:c.561G>A | NP_000528.1:p.Leu187= | |
| NM_000537.4:c.561G>A MANE Select | NP_000528.1:p.Leu187= |