Linked Data
MyVariant Identifiers:
chr17:g.39768677A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41612425A>G , CM000679.2:g.41612425A>G | GRCh38 |
| NC_000017.10:g.39768677A>G , CM000679.1:g.39768677A>G | GRCh37 |
| NC_000017.9:g.37022203A>G | NCBI36 |
| NG_008301.1:g.5403T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301653.9:c.264T>C MANE Select | ENSP00000301653.3:p.Gly88= | |
| ENST00000301653.8:c.264T>C | ENSP00000301653.3:p.Gly88= | |
| ENST00000588319.1:n.341T>C | ||
| ENST00000593067.1:c.-312-139T>C | ENSP00000467124.1:n.-312-139T>C | |
| NM_005557.3:c.264T>C | NP_005548.2:p.Gly88= | |
| NM_005557.4:c.264T>C MANE Select | NP_005548.2:p.Gly88= |