Linked Data
MyVariant Identifiers:
chr17:g.16852059T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.16948745T>C , CM000679.2:g.16948745T>C | GRCh38 |
| NC_000017.10:g.16852059T>C , CM000679.1:g.16852059T>C | GRCh37 |
| NC_000017.9:g.16792784T>C | NCBI36 |
| NG_007281.1:g.28344A>G , LRG_120:g.28344A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261652.7:c.438A>G MANE Select | ENSP00000261652.2:p.Ala146= | |
| ENST00000261652.6:c.438A>G | ENSP00000261652.2:p.Ala146= | |
| ENST00000579315.5:c.438A>G | ENSP00000464069.1:p.Ala146= | |
| ENST00000581616.2:n.441A>G | ||
| ENST00000582931.5:n.342A>G | ||
| ENST00000583789.1:c.300A>G | ENSP00000462952.1:p.Ala100= | |
| ENST00000584950.5:c.300A>G | ENSP00000463582.1:p.Ala100= | |
| NM_012452.2:c.438A>G , LRG_120t1:c.438A>G | NP_036584.1:p.Ala146= | |
| NM_012452.3:c.438A>G MANE Select | NP_036584.1:p.Ala146= |