Linked Data
MyVariant Identifiers:
chr2:g.29449930G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.29227064G>T , CM000664.2:g.29227064G>T | GRCh38 |
| NC_000002.11:g.29449930G>T , CM000664.1:g.29449930G>T | GRCh37 |
| NC_000002.10:g.29303434G>T | NCBI36 |
| NG_009445.1:g.699503C>A , LRG_488:g.699503C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000389048.8:c.2925C>A MANE Select | ENSP00000373700.3:p.Gly975= | |
| ENST00000431873.6:c.91C>A | ||
| ENST00000389048.7:c.2925C>A | ENSP00000373700.3:p.Gly975= | |
| ENST00000618119.4:c.1794C>A | ENSP00000482733.1:p.Gly598= | |
| NM_004304.4:c.2925C>A | NP_004295.2:p.Gly975= | |
| XM_024452778.1:c.78C>A | XP_024308546.1:p.Gly26= | |
| XR_001738688.2:n.3781C>A | ||
| NM_004304.5:c.2925C>A MANE Select | NP_004295.2:p.Gly975= |