Linked Data
MyVariant Identifiers:
chr7:g.128487902T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.128847848T>C , CM000669.2:g.128847848T>C | GRCh38 |
| NC_000007.13:g.128487902T>C , CM000669.1:g.128487902T>C | GRCh37 |
| NC_000007.12:g.128275138T>C | NCBI36 |
| NG_011807.1:g.22420T>C , LRG_870:g.22420T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000325888.13:c.4440T>C MANE Select | ENSP00000327145.8:p.Ala1480= | |
| ENST00000325888.12:c.4440T>C | ENSP00000327145.8:p.Ala1480= | |
| ENST00000346177.6:c.4440T>C | ENSP00000344002.6:p.Ala1480= | |
| NM_001127487.1:c.4440T>C | NP_001120959.1:p.Ala1480= | |
| NM_001458.4:c.4440T>C , LRG_870t1:c.4440T>C | NP_001449.3:p.Ala1480= | |
| NM_001127487.2:c.4440T>C | NP_001120959.1:p.Ala1480= | |
| NM_001458.5:c.4440T>C MANE Select | NP_001449.3:p.Ala1480= |