Linked Data
MyVariant Identifiers:
chr17:g.4835998T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.4932703T>C , CM000679.2:g.4932703T>C | GRCh38 |
| NC_000017.10:g.4835998T>C , CM000679.1:g.4835998T>C | GRCh37 |
| NC_000017.9:g.4776778T>C | NCBI36 |
| NG_008767.2:g.5409T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000329125.6:c.99T>C (GP1BA) MANE Select | ENSP00000329380.5:p.Cys33= | |
| ENST00000649830.1:c.-888+1639A>G (CHRNE) | ENSP00000496907.1:n.-888+1639A>G | |
| ENST00000329125.5:c.99T>C (GP1BA) | ENSP00000329380.5:p.Cys33= | |
| ENST00000611961.1:c.99T>C (GP1BA) | ENSP00000484439.1:p.Cys33= | |
| NM_000173.6:c.99T>C (GP1BA) | NP_000164.5:p.Cys33= | |
| NM_000173.7:c.99T>C (GP1BA) MANE Select | NP_000164.5:p.Cys33= |