Linked Data
MyVariant Identifiers:
chr2:g.189859798T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.188995072T>A , CM000664.2:g.188995072T>A | GRCh38 |
| NC_000002.11:g.189859798T>A , CM000664.1:g.189859798T>A | GRCh37 |
| NC_000002.10:g.189568043T>A | NCBI36 |
| NG_007404.1:g.25700T>A , LRG_3:g.25700T>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000450867.2:c.1383T>A | ENSP00000415346.2:p.Ala461= | |
| ENST00000304636.9:c.1482T>A MANE Select | ENSP00000304408.4:p.Ala494= | |
| ENST00000304636.7:c.1482T>A | ENSP00000304408.3:p.Ala494= | |
| ENST00000317840.9:c.1482T>A | ENSP00000315243.6:p.Ala494= | |
| NM_000090.3:c.1482T>A , LRG_3t1:c.1482T>A | NP_000081.1:p.Ala494= | |
| NM_000090.4:c.1482T>A MANE Select | NP_000081.2:p.Ala494= |