Linked Data
MyVariant Identifiers:
chr5:g.110412741C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.111077043C>G , CM000667.2:g.111077043C>G | GRCh38 |
| NC_000005.9:g.110412741C>G , CM000667.1:g.110412741C>G | GRCh37 |
| NC_000005.8:g.110440640C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344895.4:c.*969C>G MANE Select | ENSP00000339804.3:n.*969C>G | |
| ENST00000379706.4:c.*969C>G | ENSP00000427827.1:n.*969C>G | |
| NM_033035.4:c.*969C>G | NP_149024.1:n.*969C>G | |
| NM_138551.4:c.*969C>G | NP_612561.2:n.*969C>G | |
| NR_045089.1:n.2853C>G | ||
| NM_033035.5:c.*969C>G MANE Select | NP_149024.1:n.*969C>G | |
| NM_138551.5:c.*969C>G | NP_612561.2:n.*969C>G | |
| NR_045089.2:n.2871C>G |