Linked Data
MyVariant Identifiers:
chr2:g.189871674C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.189006948C>G , CM000664.2:g.189006948C>G | GRCh38 |
| NC_000002.11:g.189871674C>G , CM000664.1:g.189871674C>G | GRCh37 |
| NC_000002.10:g.189579919C>G | NCBI36 |
| NG_007404.1:g.37576C>G , LRG_3:g.37576C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000450867.2:c.3114C>G | ENSP00000415346.2:p.Gly1038= | |
| ENST00000304636.9:c.3213C>G MANE Select | ENSP00000304408.4:p.Gly1071= | |
| ENST00000304636.7:c.3213C>G | ENSP00000304408.3:p.Gly1071= | |
| ENST00000317840.9:c.2528-1106C>G | ENSP00000315243.6:n.2528-1106C>G | |
| NM_000090.3:c.3213C>G , LRG_3t1:c.3213C>G | NP_000081.1:p.Gly1071= | |
| NM_000090.4:c.3213C>G MANE Select | NP_000081.2:p.Gly1071= |