Linked Data
MyVariant Identifiers:
chr17:g.39768641A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41612389A>C , CM000679.2:g.41612389A>C | GRCh38 |
| NC_000017.10:g.39768641A>C , CM000679.1:g.39768641A>C | GRCh37 |
| NC_000017.9:g.37022167A>C | NCBI36 |
| NG_008301.1:g.5439T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301653.9:c.300T>G MANE Select | ENSP00000301653.3:p.Ala100= | |
| ENST00000301653.8:c.300T>G | ENSP00000301653.3:p.Ala100= | |
| ENST00000588319.1:n.377T>G | ||
| ENST00000593067.1:c.-312-103T>G | ENSP00000467124.1:n.-312-103T>G | |
| NM_005557.3:c.300T>G | NP_005548.2:p.Ala100= | |
| NM_005557.4:c.300T>G MANE Select | NP_005548.2:p.Ala100= |