Linked Data
MyVariant Identifiers:
chr11:g.112099389T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.112228666T>C , CM000673.2:g.112228666T>C | GRCh38 |
| NC_000011.9:g.112099389T>C , CM000673.1:g.112099389T>C | GRCh37 |
| NC_000011.8:g.111604599T>C | NCBI36 |
| NG_008743.1:g.7302T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000280362.8:c.156T>C MANE Select | ENSP00000280362.3:p.Asn52= | |
| ENST00000280362.7:c.156T>C | ENSP00000280362.3:p.Asn52= | |
| ENST00000524931.1:c.-49T>C | ENSP00000434688.1:n.-49T>C | |
| ENST00000525645.1:n.231T>C | ||
| ENST00000525803.1:c.156T>C | ENSP00000431750.1:p.Asn52= | |
| ENST00000528679.5:c.156T>C | ENSP00000435895.1:p.Asn52= | |
| ENST00000531673.5:c.156T>C | ENSP00000433469.1:p.Asn52= | |
| NM_000317.2:c.156T>C | NP_000308.1:p.Asn52= | |
| NM_000317.3:c.156T>C MANE Select | NP_000308.1:p.Asn52= |