Linked Data
MyVariant Identifiers:
chr8:g.19813389C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.19955878C>A , CM000670.2:g.19955878C>A | GRCh38 |
| NC_000008.10:g.19813389C>A , CM000670.1:g.19813389C>A | GRCh37 |
| NC_000008.9:g.19857669C>A | NCBI36 |
| NG_008855.1:g.21808C>A | |
| NG_008855.2:g.59162C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650287.1:c.813C>A MANE Select | ENSP00000497642.1:p.Ser271= | |
| ENST00000311322.8:c.813C>A | ENSP00000309757.6:p.Ser271= | |
| NM_000237.2:c.813C>A | NP_000228.1:p.Ser271= | |
| NM_000237.3:c.813C>A MANE Select | NP_000228.1:p.Ser271= |