Linked Data
ClinVar Variation Id:
2844618
ClinVar RCV Id:
RCV003716926
dbSNP Id:
rs1750254142
gnomAD v4:
5-132313786-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.132313786G>A , CM000667.2:g.132313786G>A | GRCh38 |
| NC_000005.9:g.131649479G>A , CM000667.1:g.131649479G>A | GRCh37 |
| NC_000005.8:g.131677378G>A | NCBI36 |
| NG_012129.1:g.24335G>A | |
| NG_012129.2:g.24335G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000200652.4:c.652+18G>A (SLC22A4) MANE Select | ENSP00000200652.3:n.652+18G>A | |
| ENST00000200652.3:c.652+18G>A (SLC22A4) | ENSP00000200652.3:n.652+18G>A | |
| ENST00000491257.1:n.456+18G>A (SLC22A4) | ||
| NM_003059.2:c.652+18G>A (SLC22A4) | NP_003050.2:n.652+18G>A | |
| NR_110997.1:n.825-1533C>T (MIR3936HG) | ||
| XM_006714675.2:c.124+18G>A (SLC22A4) | XP_006714738.1:n.124+18G>A | |
| XM_011543589.1:c.548+18G>A (SLC22A4) | XP_011541891.1:n.548+18G>A | |
| XM_006714675.4:c.124+18G>A (SLC22A4) | XP_006714738.1:n.124+18G>A | |
| XM_011543589.2:c.548+18G>A (SLC22A4) | XP_011541891.1:n.548+18G>A | |
| XM_017009776.1:c.124+18G>A (SLC22A4) | XP_016865265.1:n.124+18G>A | |
| NM_003059.3:c.652+18G>A (SLC22A4) MANE Select | NP_003050.2:n.652+18G>A |