Linked Data
MyVariant Identifiers:
chr10:g.112361468T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.110601710T>C , CM000672.2:g.110601710T>C | GRCh38 |
| NC_000010.10:g.112361468T>C , CM000672.1:g.112361468T>C | GRCh37 |
| NC_000010.9:g.112351458T>C | NCBI36 |
| NG_012217.1:g.39020T>C , LRG_774:g.39020T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684988.1:n.4951T>C | ||
| ENST00000685743.1:n.2426T>C | ||
| ENST00000686057.1:n.1069T>C | ||
| ENST00000689321.1:n.1681T>C | ||
| ENST00000689986.1:n.507T>C | ||
| ENST00000361804.5:c.2718T>C MANE Select | ENSP00000354720.5:p.Asn906= | |
| ENST00000361804.4:c.2718T>C | ENSP00000354720.4:p.Asn906= | |
| NM_005445.3:c.2718T>C , LRG_774t1:c.2718T>C | NP_005436.1:p.Asn906= | |
| NM_005445.4:c.2718T>C MANE Select | NP_005436.1:p.Asn906= |