Linked Data
MyVariant Identifiers:
chr17:g.27861141T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.29534123T>G , CM000679.2:g.29534123T>G | GRCh38 |
| NC_000017.10:g.27861141T>G , CM000679.1:g.27861141T>G | GRCh37 |
| NC_000017.9:g.24885267T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000261716.8:c.2367T>G MANE Select | ENSP00000261716.3:p.Arg789= | |
| ENST00000261716.7:c.2367T>G | ENSP00000261716.3:p.Arg789= | |
| ENST00000536202.1:c.1923T>G | ENSP00000438819.1:p.Arg641= | |
| NM_020791.2:c.2367T>G | NP_065842.1:p.Arg789= | |
| NM_025142.1:c.1923T>G | NP_079418.1:p.Arg641= | |
| XM_011525060.1:c.2367T>G | XP_011523362.1:p.Arg789= | |
| XM_011525060.2:c.2367T>G | XP_011523362.1:p.Arg789= | |
| NM_020791.4:c.2367T>G MANE Select | NP_065842.1:p.Arg789= |