Linked Data
MyVariant Identifiers:
chr17:g.40336462G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42184444G>A , CM000679.2:g.42184444G>A | GRCh38 |
| NC_000017.10:g.40336462G>A , CM000679.1:g.40336462G>A | GRCh37 |
| NC_000017.9:g.37589988G>A | NCBI36 |
| NG_011448.1:g.6009C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000293330.1:c.106C>T MANE Select | ENSP00000293330.1:p.Leu36= | |
| NM_001524.1:c.106C>T MANE Select | NP_001515.1:p.Leu36= |