Linked Data
ClinVar Variation Id:
1569998
ClinVar RCV Id:
RCV002213432
dbSNP Id:
rs2153015263
gnomAD v4:
4-987231-C-T
MyVariant Identifiers:
chr4:g.981019C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.987231C>T , CM000666.2:g.987231C>T | GRCh38 |
| NC_000004.11:g.981019C>T , CM000666.1:g.981019C>T | GRCh37 |
| NC_000004.10:g.971019C>T | NCBI36 |
| NG_008103.1:g.5235C>T | |
| NG_033042.1:g.11206G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000247933.9:c.147C>T (IDUA) | ENSP00000247933.4:p.Ser49= | |
| ENST00000514224.2:c.147C>T (IDUA) MANE Select | ENSP00000425081.2:p.Ser49= | |
| ENST00000247933.8:c.147C>T (IDUA) | ENSP00000247933.4:p.Ser49= | |
| ENST00000398520.6:c.576+3897G>A (SLC26A1) | ENSP00000381532.2:n.576+3897G>A | |
| ENST00000502910.5:c.147C>T (IDUA) | ENSP00000422952.1:p.Ser49= | |
| ENST00000504568.5:c.145C>T (IDUA) | ||
| ENST00000506561.5:n.156C>T (IDUA) | ||
| ENST00000508168.5:n.166C>T (IDUA) | ||
| ENST00000514698.5:n.188C>T (IDUA) | ||
| ENST00000622731.4:c.576+3897G>A (SLC26A1) | ENSP00000483506.1:n.576+3897G>A | |
| NM_000203.4:c.147C>T (IDUA) | NP_000194.2:p.Ser49= | |
| NM_134425.2:c.576+3897G>A (SLC26A1) | NP_602297.1:n.576+3897G>A | |
| NR_110313.1:n.235C>T (IDUA) | ||
| XM_011513459.1:c.147C>T (IDUA) | XP_011511761.1:p.Ser49= | |
| XM_011513460.1:c.147C>T (IDUA) | XP_011511762.1:p.Ser49= | |
| XR_924947.1:n.216C>T (IDUA) | ||
| NM_000203.5:c.147C>T (IDUA) MANE Select | NP_000194.2:p.Ser49= | |
| XM_017008163.1:c.-1320C>T (IDUA) | XP_016863652.1:n.-1320C>T | |
| NM_134425.3:c.576+3897G>A (SLC26A1) | NP_602297.1:n.576+3897G>A | |
| NM_134425.4:c.576+3897G>A (SLC26A1) | NP_602297.1:n.576+3897G>A |