Linked Data
MyVariant Identifiers:
chr10:g.112361441T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.110601683T>A , CM000672.2:g.110601683T>A | GRCh38 |
| NC_000010.10:g.112361441T>A , CM000672.1:g.112361441T>A | GRCh37 |
| NC_000010.9:g.112351431T>A | NCBI36 |
| NG_012217.1:g.38993T>A , LRG_774:g.38993T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684988.1:n.4924T>A | ||
| ENST00000685743.1:n.2399T>A | ||
| ENST00000686057.1:n.1042T>A | ||
| ENST00000689321.1:n.1654T>A | ||
| ENST00000689986.1:n.480T>A | ||
| ENST00000361804.5:c.2691T>A MANE Select | ENSP00000354720.5:p.Leu897= | |
| ENST00000361804.4:c.2691T>A | ENSP00000354720.4:p.Leu897= | |
| NM_005445.3:c.2691T>A , LRG_774t1:c.2691T>A | NP_005436.1:p.Leu897= | |
| NM_005445.4:c.2691T>A MANE Select | NP_005436.1:p.Leu897= |