Linked Data
MyVariant Identifiers:
chr10:g.112361900T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.110602142T>G , CM000672.2:g.110602142T>G | GRCh38 |
| NC_000010.10:g.112361900T>G , CM000672.1:g.112361900T>G | GRCh37 |
| NC_000010.9:g.112351890T>G | NCBI36 |
| NG_012217.1:g.39452T>G , LRG_774:g.39452T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684988.1:n.5302T>G | ||
| ENST00000685743.1:n.2777T>G | ||
| ENST00000686057.1:n.1420T>G | ||
| ENST00000689321.1:n.2032T>G | ||
| ENST00000689986.1:n.858T>G | ||
| ENST00000361804.5:c.3069T>G MANE Select | ENSP00000354720.5:p.Leu1023= | |
| ENST00000361804.4:c.3069T>G | ENSP00000354720.4:p.Leu1023= | |
| NM_005445.3:c.3069T>G , LRG_774t1:c.3069T>G | NP_005436.1:p.Leu1023= | |
| NM_005445.4:c.3069T>G MANE Select | NP_005436.1:p.Leu1023= |