Linked Data
MyVariant Identifiers:
chr20:g.31996618T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.33408812T>A , CM000682.2:g.33408812T>A | GRCh38 |
| NC_000020.10:g.31996618T>A , CM000682.1:g.31996618T>A | GRCh37 |
| NC_000020.9:g.31460279T>A | NCBI36 |
| NG_011622.1:g.40081A>T , LRG_332:g.40081A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000217381.3:c.1314A>T MANE Select | ENSP00000217381.2:p.Pro438= | |
| ENST00000217381.2:c.1314A>T | ENSP00000217381.2:p.Pro438= | |
| NM_003098.2:c.1314A>T , LRG_332t1:c.1314A>T | NP_003089.1:p.Pro438= | |
| XM_005260517.1:c.1314A>T | XP_005260574.1:p.Pro438= | |
| XM_011529007.1:c.1346A>T | XP_011527309.1:p.Gln449Leu | |
| XM_011529008.1:c.1346A>T | XP_011527310.1:p.Gln449Leu | |
| XR_936612.1:n.1350A>T | ||
| XM_024451971.1:c.987A>T | XP_024307739.1:p.Pro329= | |
| NM_003098.3:c.1314A>T MANE Select | NP_003089.1:p.Pro438= |