Linked Data
ClinVar Variation Id:
120307
ClinVar RCV Id:
RCV000106388
dbSNP Id:
rs587777242
gnomAD v4:
22-17191773-C-G
PubMed:
PMID:24552285
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.17191773C>G , CM000684.2:g.17191773C>G | GRCh38 |
| NC_000022.10:g.17672663C>G , CM000684.1:g.17672663C>G | GRCh37 |
| NC_000022.9:g.16052663C>G | NCBI36 |
| NG_033943.1:g.35082G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000330232.9:c.68G>C | ENSP00000332871.4:p.Trp23Ser | |
| ENST00000449907.8:c.665G>C | ENSP00000406443.2:p.Trp222Ser | |
| ENST00000543038.2:c.791G>C | ENSP00000442482.2:p.Trp264Ser | |
| ENST00000610390.5:c.431G>C | ENSP00000483418.1:p.Trp144Ser | |
| ENST00000648061.2:c.68G>C | ENSP00000496894.1:p.Trp23Ser | |
| ENST00000649310.2:c.791G>C | ENSP00000496839.2:p.Trp264Ser | |
| ENST00000649746.2:c.791G>C | ENSP00000497913.2:p.Trp264Ser | |
| ENST00000649915.2:c.*263G>C | ENSP00000497681.2:n.*263G>C | |
| ENST00000696189.1:n.92G>C | ||
| ENST00000696196.1:c.791G>C | ENSP00000512479.1:p.Trp264Ser | |
| ENST00000696197.1:c.791G>C | ENSP00000512480.1:p.Trp264Ser | |
| ENST00000696198.1:n.92G>C | ||
| ENST00000696220.1:c.38G>C | ENSP00000512486.1:p.Trp13Ser | |
| ENST00000696221.1:c.38G>C | ENSP00000512487.1:p.Trp13Ser | |
| ENST00000696222.1:c.38G>C | ENSP00000512488.1:p.Trp13Ser | |
| ENST00000696223.1:c.38G>C | ENSP00000512489.1:p.Trp13Ser | |
| ENST00000696224.1:c.185G>C | ENSP00000512490.1:p.Trp62Ser | |
| ENST00000696225.1:c.791G>C | ENSP00000512491.1:p.Trp264Ser | |
| ENST00000399837.8:c.791G>C MANE Select | ENSP00000382731.2:p.Trp264Ser | |
| ENST00000449907.7:c.665G>C | ENSP00000406443.2:p.Trp222Ser | |
| ENST00000648061.1:c.68G>C | ENSP00000496894.1:p.Trp23Ser | |
| ENST00000648668.1:n.229G>C | ||
| ENST00000649540.1:c.665G>C | ENSP00000497469.1:p.Trp222Ser | |
| ENST00000649915.1:c.654G>C | ||
| ENST00000650635.1:n.791G>C | ||
| ENST00000262607.3:c.791G>C | ENSP00000262607.2:p.Trp264Ser | |
| ENST00000330232.8:c.68G>C | ENSP00000332871.4:p.Trp23Ser | |
| ENST00000399837.6:c.791G>C | ENSP00000382731.2:p.Trp264Ser | |
| ENST00000399839.5:c.791G>C | ENSP00000382733.1:p.Trp264Ser | |
| ENST00000449907.6:c.665G>C | ENSP00000406443.2:p.Trp222Ser | |
| ENST00000480276.1:n.231G>C | ||
| ENST00000610390.4:c.431G>C | ENSP00000483418.1:p.Trp144Ser | |
| NM_001282225.1:c.791G>C | NP_001269154.1:p.Trp264Ser | |
| NM_001282226.1:c.791G>C | NP_001269155.1:p.Trp264Ser | |
| NM_001282227.1:c.665G>C | NP_001269156.1:p.Trp222Ser | |
| NM_001282228.1:c.665G>C | NP_001269157.1:p.Trp222Ser | |
| NM_001282229.1:c.431G>C | NP_001269158.1:p.Trp144Ser | |
| NM_177405.2:c.68G>C | NP_803124.1:p.Trp23Ser | |
| XM_006724080.2:c.-1544G>C | XP_006724143.1:n.-1544G>C | |
| XM_011546133.1:c.791G>C | XP_011544435.1:p.Trp264Ser | |
| NM_001282225.2:c.791G>C MANE Select | NP_001269154.1:p.Trp264Ser | |
| XM_006724080.3:c.-1544G>C | XP_006724143.1:n.-1544G>C | |
| XM_011546133.2:c.791G>C | XP_011544435.1:p.Trp264Ser | |
| NM_001282226.2:c.791G>C | NP_001269155.1:p.Trp264Ser | |
| NM_001282227.2:c.665G>C | NP_001269156.1:p.Trp222Ser | |
| NM_001282228.2:c.665G>C | NP_001269157.1:p.Trp222Ser | |
| NM_177405.3:c.68G>C | NP_803124.1:p.Trp23Ser | |
| NM_001282229.2:c.431G>C | NP_001269158.1:p.Trp144Ser |