Linked Data
MyVariant Identifiers:
chr20:g.30407939T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.31820136T>C , CM000682.2:g.31820136T>C | GRCh38 |
| NC_000020.10:g.30407939T>C , CM000682.1:g.30407939T>C | GRCh37 |
| NC_000020.9:g.29871600T>C | NCBI36 |
| NG_012847.1:g.5762T>C , LRG_392:g.5762T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375985.5:c.63T>C MANE Select | ENSP00000365152.4:p.Pro21= | |
| ENST00000375985.4:c.63T>C | ENSP00000365152.4:p.Pro21= | |
| ENST00000375994.6:c.63T>C | ENSP00000365162.2:p.Pro21= | |
| NM_033118.3:c.63T>C , LRG_392t1:c.63T>C | NP_149109.1:p.Pro21= | |
| XR_244155.1:n.228T>C | ||
| NM_033118.4:c.63T>C MANE Select | NP_149109.1:p.Pro21= |