Linked Data
MyVariant Identifiers:
chr10:g.112361831A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.110602073A>G , CM000672.2:g.110602073A>G | GRCh38 |
| NC_000010.10:g.112361831A>G , CM000672.1:g.112361831A>G | GRCh37 |
| NC_000010.9:g.112351821A>G | NCBI36 |
| NG_012217.1:g.39383A>G , LRG_774:g.39383A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684988.1:n.5233A>G | ||
| ENST00000685743.1:n.2708A>G | ||
| ENST00000686057.1:n.1351A>G | ||
| ENST00000689321.1:n.1963A>G | ||
| ENST00000689986.1:n.789A>G | ||
| ENST00000361804.5:c.3000A>G MANE Select | ENSP00000354720.5:p.Leu1000= | |
| ENST00000361804.4:c.3000A>G | ENSP00000354720.4:p.Leu1000= | |
| NM_005445.3:c.3000A>G , LRG_774t1:c.3000A>G | NP_005436.1:p.Leu1000= | |
| NM_005445.4:c.3000A>G MANE Select | NP_005436.1:p.Leu1000= |