Linked Data
MyVariant Identifiers:
chr19:g.12997916T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.12887102T>C , CM000681.2:g.12887102T>C | GRCh38 |
| NC_000019.9:g.12997916T>C , CM000681.1:g.12997916T>C | GRCh37 |
| NC_000019.8:g.12858916T>C | NCBI36 |
| NG_009292.1:g.943T>C | |
| NG_013087.1:g.5102A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264834.6:c.39A>G MANE Select | ENSP00000264834.3:p.Thr13= | |
| ENST00000264834.4:c.39A>G | ENSP00000264834.3:p.Thr13= | |
| NM_006563.3:c.39A>G | NP_006554.1:p.Thr13= | |
| XM_011527642.1:c.-165A>G | XP_011525944.1:n.-165A>G | |
| NM_006563.4:c.39A>G | NP_006554.1:p.Thr13= | |
| XM_011527642.2:c.-165A>G | XP_011525944.1:n.-165A>G | |
| NM_006563.5:c.39A>G MANE Select | NP_006554.1:p.Thr13= |