Linked Data
MyVariant Identifiers:
chr1:g.160099996C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.160130206C>A , CM000663.2:g.160130206C>A | GRCh38 |
| NC_000001.10:g.160099996C>A , CM000663.1:g.160099996C>A | GRCh37 |
| NC_000001.9:g.158366620C>A | NCBI36 |
| NG_008014.1:g.19449C>A , LRG_6:g.19449C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361216.8:c.1566C>A MANE Select | ENSP00000354490.3:p.Gly522= | |
| ENST00000361216.7:c.1566C>A | ENSP00000354490.3:p.Gly522= | |
| ENST00000392233.7:c.1566C>A | ENSP00000376066.3:p.Gly522= | |
| ENST00000447527.1:c.698C>A | ||
| ENST00000472488.5:n.1669C>A | ||
| NM_000702.3:c.1566C>A | NP_000693.1:p.Gly522= | |
| NM_000702.4:c.1566C>A MANE Select | NP_000693.1:p.Gly522= |