Linked Data
MyVariant Identifiers:
chr19:g.12997928G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.12887114G>C , CM000681.2:g.12887114G>C | GRCh38 |
| NC_000019.9:g.12997928G>C , CM000681.1:g.12997928G>C | GRCh37 |
| NC_000019.8:g.12858928G>C | NCBI36 |
| NG_009292.1:g.955G>C | |
| NG_013087.1:g.5090C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264834.6:c.27C>G MANE Select | ENSP00000264834.3:p.Pro9= | |
| ENST00000264834.4:c.27C>G | ENSP00000264834.3:p.Pro9= | |
| NM_006563.3:c.27C>G | NP_006554.1:p.Pro9= | |
| XM_011527642.1:c.-177C>G | XP_011525944.1:n.-177C>G | |
| NM_006563.4:c.27C>G | NP_006554.1:p.Pro9= | |
| XM_011527642.2:c.-177C>G | XP_011525944.1:n.-177C>G | |
| NM_006563.5:c.27C>G MANE Select | NP_006554.1:p.Pro9= |