Linked Data
MyVariant Identifiers:
chr12:g.21353581T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.21200647T>A , CM000674.2:g.21200647T>A | GRCh38 |
| NC_000012.11:g.21353581T>A , CM000674.1:g.21353581T>A | GRCh37 |
| NC_000012.10:g.21244848T>A | NCBI36 |
| NG_011745.1:g.74454T>A , LRG_1022:g.74454T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000256958.3:c.1110T>A MANE Select | ENSP00000256958.2:p.Pro370= | |
| ENST00000256958.2:c.1110T>A | ENSP00000256958.2:p.Pro370= | |
| NM_006446.4:c.1110T>A , LRG_1022t1:c.1110T>A | NP_006437.3:p.Pro370= | |
| NM_006446.5:c.1110T>A MANE Select | NP_006437.3:p.Pro370= |