Linked Data
MyVariant Identifiers:
chr6:g.32411116C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32443339C>G , CM000668.2:g.32443339C>G | GRCh38 |
| NC_000006.11:g.32411116C>G , CM000668.1:g.32411116C>G | GRCh37 |
| NC_000006.10:g.32519094C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000395388.7:c.483C>G MANE Select | ENSP00000378786.2:p.Val161= | |
| ENST00000374982.5:c.408C>G | ENSP00000364121.5:p.Val136= | |
| ENST00000395388.6:c.483C>G | ENSP00000378786.2:p.Val161= | |
| NM_019111.4:c.483C>G | NP_061984.2:p.Val161= | |
| NM_019111.5:c.483C>G MANE Select | NP_061984.2:p.Val161= |