Linked Data
ClinVar Variation Id:
7122
ClinVar RCV Id:
RCV000007542
RCV000506601
RCV000763575
RCV000781237
RCV001004260
RCV001831525
RCV003137499
dbSNP Id:
rs74597325
ExAC:
7:117227865 C / T
gnomAD v2:
7-117227865-C-T
gnomAD v3:
7-117587811-C-T
gnomAD v4:
7-117587811-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.117587811C>T , CM000669.2:g.117587811C>T | GRCh38 |
| NC_000007.13:g.117227865C>T , CM000669.1:g.117227865C>T | GRCh37 |
| NC_000007.12:g.117015101C>T | NCBI36 |
| NG_016465.4:g.127028C>T , LRG_663:g.127028C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647720.2:c.1657C>T | ENSP00000497673.2:p.Arg553Ter | |
| ENST00000647978.2:c.*1371C>T | ENSP00000497658.1:n.*1371C>T | |
| ENST00000649781.2:c.1474C>T | ENSP00000497203.1:p.Arg492Ter | |
| ENST00000685018.2:c.1657C>T | ENSP00000510194.2:p.Arg553Ter | |
| ENST00000687278.2:c.1657C>T | ENSP00000509593.2:p.Arg553Ter | |
| ENST00000699585.1:c.1657C>T | ENSP00000514456.1:p.Arg553Ter | |
| ENST00000699598.1:c.1657C>T | ENSP00000514467.1:p.Arg553Ter | |
| ENST00000699599.1:c.1657C>T | ENSP00000514468.1:p.Arg553Ter | |
| ENST00000699600.1:c.1657C>T | ENSP00000514469.1:p.Arg553Ter | |
| ENST00000699601.1:c.1657C>T | ENSP00000514470.1:p.Arg553Ter | |
| ENST00000699602.1:c.1657C>T | ENSP00000514471.1:p.Arg553Ter | |
| ENST00000699604.1:c.*1481C>T | ENSP00000514472.1:n.*1481C>T | |
| ENST00000699605.1:c.1231C>T | ENSP00000514473.1:p.Arg411Ter | |
| ENST00000003084.11:c.1657C>T MANE Select | ENSP00000003084.6:p.Arg553Ter | |
| ENST00000647978.1:c.*1371C>T | ENSP00000497658.1:n.*1371C>T | |
| ENST00000648260.1:c.1402-15015C>T | ENSP00000497957.1:n.1402-15015C>T | |
| ENST00000649406.1:c.1474C>T | ENSP00000497965.1:p.Arg492Ter | |
| ENST00000649781.1:c.1474C>T | ENSP00000497203.1:p.Arg492Ter | |
| ENST00000003084.10:c.1657C>T | ENSP00000003084.6:p.Arg553Ter | |
| ENST00000426809.5:c.1567C>T | ENSP00000389119.1:p.Arg523Ter | |
| NM_000492.3:c.1657C>T , LRG_663t1:c.1657C>T | NP_000483.3:p.Arg553Ter | |
| XM_011515751.1:c.1747C>T | XP_011514053.1:p.Arg583Ter | |
| XM_011515752.1:c.1747C>T | XP_011514054.1:p.Arg583Ter | |
| XM_011515753.1:c.1414C>T | XP_011514055.1:p.Arg472Ter | |
| XM_011515754.1:c.1414C>T | XP_011514056.1:p.Arg472Ter | |
| NM_000492.4:c.1657C>T MANE Select | NP_000483.3:p.Arg553Ter |