Linked Data
MyVariant Identifiers:
chr13:g.33628140T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.33054003T>C , CM000675.2:g.33054003T>C | GRCh38 |
| NC_000013.10:g.33628140T>C , CM000675.1:g.33628140T>C | GRCh37 |
| NC_000013.9:g.32526140T>C | NCBI36 |
| NG_011485.1:g.42570T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000380099.4:c.1056T>C MANE Select | ENSP00000369442.3:p.Phe352= | |
| ENST00000380099.3:c.1056T>C | ENSP00000369442.3:p.Phe352= | |
| ENST00000487852.1:n.1064T>C | ||
| NM_004795.3:c.1056T>C | NP_004786.2:p.Phe352= | |
| XM_006719895.1:c.135T>C | XP_006719958.1:p.Phe45= | |
| XM_006719895.2:c.135T>C | XP_006719958.1:p.Phe45= | |
| NM_004795.4:c.1056T>C MANE Select | NP_004786.2:p.Phe352= |