Linked Data
MyVariant Identifiers:
chr17:g.7919122G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8015804G>C , CM000679.2:g.8015804G>C | GRCh38 |
| NC_000017.10:g.7919122G>C , CM000679.1:g.7919122G>C | GRCh37 |
| NC_000017.9:g.7859847G>C | NCBI36 |
| NG_009092.1:g.18135G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000254854.5:c.3006G>C MANE Select | ENSP00000254854.4:p.Thr1002= | |
| ENST00000254854.4:c.3006G>C | ENSP00000254854.4:p.Thr1002= | |
| NM_000180.3:c.3006G>C | NP_000171.1:p.Thr1002= | |
| XM_011523816.1:c.3006G>C | XP_011522118.1:p.Thr1002= | |
| NM_000180.4:c.3006G>C MANE Select | NP_000171.1:p.Thr1002= |