Linked Data
MyVariant Identifiers:
chr19:g.15295146A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.15184335A>C , CM000681.2:g.15184335A>C | GRCh38 |
| NC_000019.9:g.15295146A>C , CM000681.1:g.15295146A>C | GRCh37 |
| NC_000019.8:g.15156146A>C | NCBI36 |
| NG_009819.1:g.21647T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263388.7:c.2526T>G MANE Select | ENSP00000263388.1:p.Thr842= | |
| ENST00000263388.6:c.2526T>G | ENSP00000263388.1:p.Thr842= | |
| ENST00000601011.1:c.2407+571T>G | ENSP00000473138.1:n.2407+571T>G | |
| NM_000435.2:c.2526T>G | NP_000426.2:p.Thr842= | |
| XM_005259924.3:c.2410+571T>G | XP_005259981.1:n.2410+571T>G | |
| XM_005259924.4:c.2410+571T>G | XP_005259981.1:n.2410+571T>G | |
| NM_000435.3:c.2526T>G MANE Select | NP_000426.2:p.Thr842= |