Linked Data
dbSNP Id:
rs1391208713
gnomAD v2:
2-29445102-G-A
gnomAD v3:
2-29222236-G-A
gnomAD v4:
2-29222236-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.29222236G>A , CM000664.2:g.29222236G>A | GRCh38 |
| NC_000002.11:g.29445102G>A , CM000664.1:g.29445102G>A | GRCh37 |
| NC_000002.10:g.29298606G>A | NCBI36 |
| NG_009445.1:g.704331C>T , LRG_488:g.704331C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000389048.8:c.3515+108C>T MANE Select | ENSP00000373700.3:n.3515+108C>T | |
| ENST00000431873.6:c.742+108C>T | ||
| ENST00000638605.1:n.392+108C>T | ||
| ENST00000642122.1:c.311+108C>T | ENSP00000493203.1:n.311+108C>T | |
| ENST00000389048.7:c.3515+108C>T | ENSP00000373700.3:n.3515+108C>T | |
| ENST00000431873.5:c.395+108C>T | ENSP00000414027.2:n.395+108C>T | |
| ENST00000453137.1:c.209+108C>T | ENSP00000387488.1:n.209+108C>T | |
| ENST00000618119.4:c.2384+108C>T | ENSP00000482733.1:n.2384+108C>T | |
| NM_004304.4:c.3515+108C>T | NP_004295.2:n.3515+108C>T | |
| NM_001353765.1:c.311+108C>T | NP_001340694.1:n.311+108C>T | |
| XM_024452778.1:c.668+108C>T | XP_024308546.1:n.668+108C>T | |
| XM_024452779.1:c.311+108C>T | XP_024308547.1:n.311+108C>T | |
| NM_004304.5:c.3515+108C>T MANE Select | NP_004295.2:n.3515+108C>T | |
| NM_001353765.2:c.311+108C>T | NP_001340694.1:n.311+108C>T |