Linked Data
MyVariant Identifiers:
chr5:g.110407616C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.111071918C>T , CM000667.2:g.111071918C>T | GRCh38 |
| NC_000005.9:g.110407616C>T , CM000667.1:g.110407616C>T | GRCh37 |
| NC_000005.8:g.110435515C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344895.4:c.28C>T MANE Select | ENSP00000339804.3:p.Leu10= | |
| ENST00000344895.3:c.28C>T | ENSP00000339804.3:p.Leu10= | |
| ENST00000420978.6:c.35-7C>T | ENSP00000399099.2:n.35-7C>T | |
| NM_033035.4:c.28C>T | NP_149024.1:p.Leu10= | |
| NR_045089.1:n.1439-7C>T | ||
| NM_033035.5:c.28C>T MANE Select | NP_149024.1:p.Leu10= | |
| NR_045089.2:n.1457-7C>T |