Linked Data
MyVariant Identifiers:
chr1:g.159272163T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.159302373T>C , CM000663.2:g.159302373T>C | GRCh38 |
| NC_000001.10:g.159272163T>C , CM000663.1:g.159272163T>C | GRCh37 |
| NC_000001.9:g.157538787T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000693622.1:c.9T>C MANE Select | ENSP00000509626.1:p.Pro3= | |
| ENST00000368114.1:c.9T>C | ENSP00000357096.1:p.Pro3= | |
| ENST00000368115.5:c.9T>C | ENSP00000357097.1:p.Pro3= | |
| NM_002001.3:c.9T>C | NP_001992.1:p.Pro3= | |
| NM_001387280.1:c.9T>C MANE Select | NP_001374209.1:p.Pro3= | |
| NM_001387281.1:c.9T>C | NP_001374210.1:p.Pro3= | |
| NM_001387282.1:c.9T>C | NP_001374211.1:p.Pro3= | |
| NM_002001.4:c.9T>C | NP_001992.1:p.Pro3= |