Linked Data
MyVariant Identifiers:
chr17:g.39742619A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41586367A>C , CM000679.2:g.41586367A>C | GRCh38 |
| NC_000017.10:g.39742619A>C , CM000679.1:g.39742619A>C | GRCh37 |
| NC_000017.9:g.36996145A>C | NCBI36 |
| NG_008624.1:g.5529T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000167586.7:c.468T>G MANE Select | ENSP00000167586.6:p.Pro156= | |
| ENST00000167586.6:c.468T>G | ENSP00000167586.6:p.Pro156= | |
| NM_000526.4:c.468T>G | NP_000517.2:p.Pro156= | |
| NM_000526.5:c.468T>G MANE Select | NP_000517.3:p.Pro156= |