Linked Data
MyVariant Identifiers:
chr10:g.101605386T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.99845629T>G , CM000672.2:g.99845629T>G | GRCh38 |
| NC_000010.10:g.101605386T>G , CM000672.1:g.101605386T>G | GRCh37 |
| NC_000010.9:g.101595376T>G | NCBI36 |
| NG_011798.1:g.67924T>G | |
| NG_011798.2:g.68032T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647814.1:c.3993T>G MANE Select | ENSP00000497274.1:p.Gly1331= | |
| ENST00000649459.1:n.341T>G | ||
| ENST00000370449.8:c.3993T>G | ENSP00000359478.4:p.Gly1331= | |
| NM_000392.4:c.3993T>G | NP_000383.1:p.Gly1331= | |
| XM_006717630.2:c.3297T>G | XP_006717693.1:p.Gly1099= | |
| XR_945604.1:n.4177-54T>G | ||
| XR_945605.1:n.4057T>G | ||
| NM_000392.5:c.3993T>G MANE Select | NP_000383.2:p.Gly1331= | |
| XM_006717630.3:c.3297T>G | XP_006717693.1:p.Gly1099= | |
| XR_945604.3:n.4231-54T>G | ||
| XR_945605.3:n.4109T>G |