Linked Data
MyVariant Identifiers:
chr8:g.119945276A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.118933037A>G , CM000670.2:g.118933037A>G | GRCh38 |
| NC_000008.10:g.119945276A>G , CM000670.1:g.119945276A>G | GRCh37 |
| NC_000008.9:g.120014457A>G | NCBI36 |
| NG_012202.1:g.24108T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297350.9:c.294T>C MANE Select | ENSP00000297350.4:p.Asn98= | |
| ENST00000297350.8:c.294T>C | ENSP00000297350.4:p.Asn98= | |
| ENST00000517352.1:c.294T>C | ENSP00000427924.1:p.Asn98= | |
| NM_002546.3:c.294T>C | NP_002537.3:p.Asn98= | |
| NM_002546.4:c.294T>C MANE Select | NP_002537.3:p.Asn98= |