Linked Data
dbSNP Id:
rs1467248823
gnomAD v2:
19-39200838-A-G
gnomAD v3:
19-38710198-A-G
gnomAD v4:
19-38710198-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.38710198A>G , CM000681.2:g.38710198A>G | GRCh38 |
| NC_000019.9:g.39200838A>G , CM000681.1:g.39200838A>G | GRCh37 |
| NC_000019.8:g.43892678A>G | NCBI36 |
| NG_007082.2:g.67512A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000440400.3:c.733+722A>G | ENSP00000398393.2:n.733+722A>G | |
| ENST00000697712.1:c.593-59A>G | ENSP00000513410.1:n.593-59A>G | |
| ENST00000252699.7:c.734-59A>G MANE Select | ENSP00000252699.2:n.734-59A>G | |
| ENST00000424234.7:c.733+722A>G | ENSP00000411187.4:n.733+722A>G | |
| ENST00000440400.2:c.733+722A>G | ENSP00000398393.2:n.733+722A>G | |
| ENST00000252699.6:c.734-59A>G | ENSP00000252699.2:n.734-59A>G | |
| ENST00000390009.7:c.163-4271A>G | ENSP00000439497.1:n.163-4271A>G | |
| ENST00000424234.6:c.272+9489A>G | ENSP00000411187.3:n.272+9489A>G | |
| ENST00000586538.1:c.136+722A>G | ENSP00000465176.1:n.136+722A>G | |
| ENST00000588618.5:n.831-59A>G | ||
| ENST00000589528.1:c.285+9484A>G | ||
| NM_004924.4:c.734-59A>G | NP_004915.2:n.734-59A>G | |
| XM_005259281.3:c.734-59A>G | XP_005259338.1:n.734-59A>G | |
| XM_005259282.3:c.733+722A>G | XP_005259339.1:n.733+722A>G | |
| XM_006723406.1:c.733+722A>G | XP_006723469.1:n.733+722A>G | |
| NM_001322033.1:c.733+722A>G | NP_001308962.1:n.733+722A>G | |
| NM_004924.5:c.734-59A>G | NP_004915.2:n.734-59A>G | |
| XM_005259281.5:c.734-59A>G | XP_005259338.1:n.734-59A>G | |
| XM_006723406.3:c.733+722A>G | XP_006723469.1:n.733+722A>G | |
| XM_017027331.2:c.734-59A>G | XP_016882820.1:n.734-59A>G | |
| XR_001753937.1:n.123-8034T>C | ||
| NM_004924.6:c.734-59A>G MANE Select | NP_004915.2:n.734-59A>G | |
| NM_001322033.2:c.733+722A>G | NP_001308962.1:n.733+722A>G |