Linked Data
MyVariant Identifiers:
chr2:g.84652590T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.84425466T>A , CM000664.2:g.84425466T>A | GRCh38 |
| NC_000002.11:g.84652590T>A , CM000664.1:g.84652590T>A | GRCh37 |
| NC_000002.10:g.84506101T>A | NCBI36 |
| NG_016755.1:g.38997A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000393868.7:c.963A>T MANE Select | ENSP00000377446.2:p.Ala321= | |
| ENST00000651342.1:c.*403A>T | ENSP00000498471.1:n.*403A>T | |
| ENST00000393868.6:c.963A>T | ENSP00000377446.2:p.Ala321= | |
| ENST00000484365.1:n.1471A>T | ||
| ENST00000487809.1:n.710A>T | ||
| ENST00000491123.5:n.809A>T | ||
| NM_003849.3:c.963A>T | NP_003840.2:p.Ala321= | |
| NM_003849.4:c.963A>T MANE Select | NP_003840.2:p.Ala321= |