Linked Data
MyVariant Identifiers:
chr13:g.33628054C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.33053917C>T , CM000675.2:g.33053917C>T | GRCh38 |
| NC_000013.10:g.33628054C>T , CM000675.1:g.33628054C>T | GRCh37 |
| NC_000013.9:g.32526054C>T | NCBI36 |
| NG_011485.1:g.42484C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000380099.4:c.970C>T MANE Select | ENSP00000369442.3:p.Leu324= | |
| ENST00000380099.3:c.970C>T | ENSP00000369442.3:p.Leu324= | |
| ENST00000487852.1:n.978C>T | ||
| NM_004795.3:c.970C>T | NP_004786.2:p.Leu324= | |
| XM_006719895.1:c.49C>T | XP_006719958.1:p.Leu17= | |
| XM_006719895.2:c.49C>T | XP_006719958.1:p.Leu17= | |
| NM_004795.4:c.970C>T MANE Select | NP_004786.2:p.Leu324= |