Linked Data
dbSNP Id:
rs779493006
ExAC:
5:131676233 T / A
gnomAD v2:
5-131676233-T-A
gnomAD v3:
5-132340540-T-A
gnomAD v4:
5-132340540-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.132340540T>A , CM000667.2:g.132340540T>A | GRCh38 |
| NC_000005.9:g.131676233T>A , CM000667.1:g.131676233T>A | GRCh37 |
| NC_000005.8:g.131704132T>A | NCBI36 |
| NG_012129.1:g.51089T>A | |
| NG_012129.2:g.51089T>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000200652.4:c.1445-25T>A (SLC22A4) MANE Select | ENSP00000200652.3:n.1445-25T>A | |
| ENST00000200652.3:c.1445-25T>A (SLC22A4) | ENSP00000200652.3:n.1445-25T>A | |
| NM_003059.2:c.1445-25T>A (SLC22A4) | NP_003050.2:n.1445-25T>A | |
| NR_110997.1:n.561-5614A>T (MIR3936HG) | ||
| XM_006714675.2:c.917-25T>A (SLC22A4) | XP_006714738.1:n.917-25T>A | |
| XM_011543589.1:c.1169-25T>A (SLC22A4) | XP_011541891.1:n.1169-25T>A | |
| XM_006714675.4:c.917-25T>A (SLC22A4) | XP_006714738.1:n.917-25T>A | |
| XM_011543589.2:c.1169-25T>A (SLC22A4) | XP_011541891.1:n.1169-25T>A | |
| XM_017009776.1:c.917-25T>A (SLC22A4) | XP_016865265.1:n.917-25T>A | |
| NM_003059.3:c.1445-25T>A (SLC22A4) MANE Select | NP_003050.2:n.1445-25T>A |