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