Linked Data
MyVariant Identifiers:
chr20:g.6750791C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.6770144C>G , CM000682.2:g.6770144C>G | GRCh38 |
| NC_000020.10:g.6750791C>G , CM000682.1:g.6750791C>G | GRCh37 |
| NC_000020.9:g.6698791C>G | NCBI36 |
| NG_023233.1:g.7047C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378827.5:c.18C>G MANE Select | ENSP00000368104.3:p.Arg6= | |
| ENST00000378827.4:c.18C>G | ENSP00000368104.3:p.Arg6= | |
| NM_001200.2:c.18C>G | NP_001191.1:p.Arg6= | |
| XM_011529323.1:c.-123+1269C>G | XP_011527625.1:n.-123+1269C>G | |
| NM_001200.3:c.18C>G | NP_001191.1:p.Arg6= | |
| NM_001200.4:c.18C>G MANE Select | NP_001191.1:p.Arg6= |