Linked Data
MyVariant Identifiers:
chr8:g.63985500T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.63072941T>G , CM000670.2:g.63072941T>G | GRCh38 |
| NC_000008.10:g.63985500T>G , CM000670.1:g.63985500T>G | GRCh37 |
| NC_000008.9:g.64148054T>G | NCBI36 |
| NG_016123.1:g.18113A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260116.5:c.352A>C MANE Select | ENSP00000260116.4:p.Arg118= | |
| ENST00000260116.4:c.352A>C | ENSP00000260116.4:p.Arg118= | |
| ENST00000521138.1:n.232+12877A>C | ||
| NM_000370.3:c.352A>C MANE Select | NP_000361.1:p.Arg118= | |
| XM_006716468.2:c.205-8625A>C | XP_006716531.1:n.205-8625A>C | |
| XM_006716468.4:c.205-8625A>C | XP_006716531.1:n.205-8625A>C |