Linked Data
MyVariant Identifiers:
chr17:g.39768512G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41612260G>C , CM000679.2:g.41612260G>C | GRCh38 |
| NC_000017.10:g.39768512G>C , CM000679.1:g.39768512G>C | GRCh37 |
| NC_000017.9:g.37022038G>C | NCBI36 |
| NG_008301.1:g.5568C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301653.9:c.429C>G MANE Select | ENSP00000301653.3:p.Ala143= | |
| ENST00000301653.8:c.429C>G | ENSP00000301653.3:p.Ala143= | |
| ENST00000588319.1:n.506C>G | ||
| ENST00000593067.1:c.-286C>G | ENSP00000467124.1:n.-286C>G | |
| NM_005557.3:c.429C>G | NP_005548.2:p.Ala143= | |
| NM_005557.4:c.429C>G MANE Select | NP_005548.2:p.Ala143= |