Linked Data
MyVariant Identifiers:
chr17:g.64224277C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.66228159C>T , CM000679.2:g.66228159C>T | GRCh38 |
| NC_000017.10:g.64224277C>T , CM000679.1:g.64224277C>T | GRCh37 |
| NC_000017.9:g.61654739C>T | NCBI36 |
| NG_012045.1:g.6280G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000205948.11:c.102G>A MANE Select | ENSP00000205948.6:p.Val34= | |
| ENST00000205948.10:c.102G>A | ENSP00000205948.6:p.Val34= | |
| ENST00000577982.1:c.102G>A | ENSP00000464301.1:p.Val34= | |
| ENST00000581797.5:c.-79G>A | ENSP00000463553.1:n.-79G>A | |
| NM_000042.2:c.102G>A | NP_000033.2:p.Val34= | |
| NM_000042.3:c.102G>A MANE Select | NP_000033.2:p.Val34= |