Linked Data
MyVariant Identifiers:
chr1:g.154543956T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.154571480T>G , CM000663.2:g.154571480T>G | GRCh38 |
| NC_000001.10:g.154543956T>G , CM000663.1:g.154543956T>G | GRCh37 |
| NC_000001.9:g.152810580T>G | NCBI36 |
| NG_008027.1:g.8700T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368476.4:c.657T>G MANE Select | ENSP00000357461.3:p.Ser219= | |
| ENST00000636034.1:c.657T>G | ENSP00000489703.1:p.Ser219= | |
| ENST00000637900.1:c.663T>G | ENSP00000490474.1:p.Ser221= | |
| ENST00000368476.3:c.657T>G | ENSP00000357461.3:p.Ser219= | |
| NM_000748.2:c.657T>G | NP_000739.1:p.Ser219= | |
| XM_017000180.2:c.147T>G | XP_016855669.1:p.Ser49= | |
| XR_001736952.2:n.909T>G | ||
| NM_000748.3:c.657T>G MANE Select | NP_000739.1:p.Ser219= |