Linked Data
MyVariant Identifiers:
chr19:g.12997946T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.12887132T>A , CM000681.2:g.12887132T>A | GRCh38 |
| NC_000019.9:g.12997946T>A , CM000681.1:g.12997946T>A | GRCh37 |
| NC_000019.8:g.12858946T>A | NCBI36 |
| NG_009292.1:g.973T>A | |
| NG_013087.1:g.5072A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264834.6:c.9A>T MANE Select | ENSP00000264834.3:p.Thr3= | |
| ENST00000264834.4:c.9A>T | ENSP00000264834.3:p.Thr3= | |
| NM_006563.3:c.9A>T | NP_006554.1:p.Thr3= | |
| NM_006563.4:c.9A>T | NP_006554.1:p.Thr3= | |
| NM_006563.5:c.9A>T MANE Select | NP_006554.1:p.Thr3= |