Linked Data
ClinVar Variation Id:
1643682
ClinVar RCV Id:
RCV002138421
dbSNP Id:
rs2116033726
gnomAD v4:
7-117592606-T-C
COSMIC:
COSM4920000
MyVariant Identifiers:
chr7:g.117232660T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.117592606T>C , CM000669.2:g.117592606T>C | GRCh38 |
| NC_000007.13:g.117232660T>C , CM000669.1:g.117232660T>C | GRCh37 |
| NC_000007.12:g.117019896T>C | NCBI36 |
| NG_016465.4:g.131823T>C , LRG_663:g.131823T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647720.2:c.2439T>C | ENSP00000497673.2:p.Ser813= | |
| ENST00000647978.2:c.*2153T>C | ENSP00000497658.1:n.*2153T>C | |
| ENST00000649781.2:c.2256T>C | ENSP00000497203.1:p.Ser752= | |
| ENST00000685018.2:c.2439T>C | ENSP00000510194.2:p.Ser813= | |
| ENST00000687278.2:c.2439T>C | ENSP00000509593.2:p.Ser813= | |
| ENST00000699585.1:c.2439T>C | ENSP00000514456.1:p.Ser813= | |
| ENST00000699598.1:c.2439T>C | ENSP00000514467.1:p.Ser813= | |
| ENST00000699599.1:c.2439T>C | ENSP00000514468.1:p.Ser813= | |
| ENST00000699600.1:c.2439T>C | ENSP00000514469.1:p.Ser813= | |
| ENST00000699601.1:c.*739T>C | ENSP00000514470.1:n.*739T>C | |
| ENST00000699602.1:c.2439T>C | ENSP00000514471.1:p.Ser813= | |
| ENST00000699604.1:c.*2263T>C | ENSP00000514472.1:n.*2263T>C | |
| ENST00000699605.1:c.2013T>C | ENSP00000514473.1:p.Ser671= | |
| ENST00000687278.1:c.30T>C | ENSP00000509593.1:p.Ser10= | |
| ENST00000003084.11:c.2439T>C MANE Select | ENSP00000003084.6:p.Ser813= | |
| ENST00000647720.1:c.89T>C | ||
| ENST00000647978.1:c.*2153T>C | ENSP00000497658.1:n.*2153T>C | |
| ENST00000648260.1:c.1402-10220T>C | ENSP00000497957.1:n.1402-10220T>C | |
| ENST00000649406.1:c.2256T>C | ENSP00000497965.1:p.Ser752= | |
| ENST00000649781.1:c.2256T>C | ENSP00000497203.1:p.Ser752= | |
| ENST00000003084.10:c.2439T>C | ENSP00000003084.6:p.Ser813= | |
| ENST00000426809.5:c.2349T>C | ENSP00000389119.1:p.Ser783= | |
| NM_000492.3:c.2439T>C , LRG_663t1:c.2439T>C | NP_000483.3:p.Ser813= | |
| XM_011515751.1:c.2529T>C | XP_011514053.1:p.Ser843= | |
| XM_011515752.1:c.2529T>C | XP_011514054.1:p.Ser843= | |
| XM_011515753.1:c.2196T>C | XP_011514055.1:p.Ser732= | |
| XM_011515754.1:c.2196T>C | XP_011514056.1:p.Ser732= | |
| NM_000492.4:c.2439T>C MANE Select | NP_000483.3:p.Ser813= |