Linked Data
MyVariant Identifiers:
chr2:g.29449840G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.29226974G>T , CM000664.2:g.29226974G>T | GRCh38 |
| NC_000002.11:g.29449840G>T , CM000664.1:g.29449840G>T | GRCh37 |
| NC_000002.10:g.29303344G>T | NCBI36 |
| NG_009445.1:g.699593C>A , LRG_488:g.699593C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000389048.8:c.3015C>A MANE Select | ENSP00000373700.3:p.Ile1005= | |
| ENST00000431873.6:c.181C>A | ||
| ENST00000389048.7:c.3015C>A | ENSP00000373700.3:p.Ile1005= | |
| ENST00000618119.4:c.1884C>A | ENSP00000482733.1:p.Ile628= | |
| NM_004304.4:c.3015C>A | NP_004295.2:p.Ile1005= | |
| XM_024452778.1:c.168C>A | XP_024308546.1:p.Ile56= | |
| XR_001738688.2:n.3871C>A | ||
| NM_004304.5:c.3015C>A MANE Select | NP_004295.2:p.Ile1005= |