Linked Data
MyVariant Identifiers:
chr19:g.18896932A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.18786122A>C , CM000681.2:g.18786122A>C | GRCh38 |
| NC_000019.9:g.18896932A>C , CM000681.1:g.18896932A>C | GRCh37 |
| NC_000019.8:g.18757932A>C | NCBI36 |
| NG_007070.1:g.10183T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000222271.7:c.1332T>G MANE Select | ENSP00000222271.2:p.Ser444= | |
| ENST00000222271.6:c.1332T>G | ENSP00000222271.2:p.Ser444= | |
| ENST00000425807.1:c.1173T>G | ENSP00000403792.1:p.Ser391= | |
| ENST00000542601.6:c.1233T>G | ENSP00000439156.2:p.Ser411= | |
| ENST00000612179.1:n.582T>G | ||
| NM_000095.2:c.1332T>G | NP_000086.2:p.Ser444= | |
| NM_000095.3:c.1332T>G MANE Select | NP_000086.2:p.Ser444= |