Linked Data
MyVariant Identifiers:
chr5:g.110407597T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.111071899T>C , CM000667.2:g.111071899T>C | GRCh38 |
| NC_000005.9:g.110407597T>C , CM000667.1:g.110407597T>C | GRCh37 |
| NC_000005.8:g.110435496T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344895.4:c.9T>C MANE Select | ENSP00000339804.3:p.Pro3= | |
| ENST00000344895.3:c.9T>C | ENSP00000339804.3:p.Pro3= | |
| ENST00000420978.6:c.35-26T>C | ENSP00000399099.2:n.35-26T>C | |
| NM_033035.4:c.9T>C | NP_149024.1:p.Pro3= | |
| NR_045089.1:n.1439-26T>C | ||
| NM_033035.5:c.9T>C MANE Select | NP_149024.1:p.Pro3= | |
| NR_045089.2:n.1457-26T>C |