Linked Data
ClinVar Variation Id:
35864
ClinVar RCV Id:
RCV000029519
RCV000724157
RCV001831610
RCV002482911
RCV001000469
RCV001004294
RCV001009368
RCV003473139
dbSNP Id:
rs76151804
ExAC:
7:117251609 A / G
gnomAD v2:
7-117251609-A-G
gnomAD v3:
7-117611555-A-G
gnomAD v4:
7-117611555-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.117611555A>G , CM000669.2:g.117611555A>G | GRCh38 |
| NC_000007.13:g.117251609A>G , CM000669.1:g.117251609A>G | GRCh37 |
| NC_000007.12:g.117038845A>G | NCBI36 |
| NG_016465.4:g.150772A>G , LRG_663:g.150772A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647720.2:c.3140-26A>G | ENSP00000497673.2:n.3140-26A>G | |
| ENST00000647978.2:c.*2854-26A>G | ENSP00000497658.1:n.*2854-26A>G | |
| ENST00000649781.2:c.2957-26A>G | ENSP00000497203.1:n.2957-26A>G | |
| ENST00000685018.2:c.3140-26A>G | ENSP00000510194.2:n.3140-26A>G | |
| ENST00000687278.2:c.3140-26A>G | ENSP00000509593.2:n.3140-26A>G | |
| ENST00000699585.1:c.3140-26A>G | ENSP00000514456.1:n.3140-26A>G | |
| ENST00000699598.1:c.3140-26A>G | ENSP00000514467.1:n.3140-26A>G | |
| ENST00000699599.1:c.3140-26A>G | ENSP00000514468.1:n.3140-26A>G | |
| ENST00000699600.1:c.3140-26A>G | ENSP00000514469.1:n.3140-26A>G | |
| ENST00000699601.1:c.*1440-26A>G | ENSP00000514470.1:n.*1440-26A>G | |
| ENST00000699602.1:c.3140-26A>G | ENSP00000514471.1:n.3140-26A>G | |
| ENST00000699604.1:c.*2964-26A>G | ENSP00000514472.1:n.*2964-26A>G | |
| ENST00000699605.1:c.2714-26A>G | ENSP00000514473.1:n.2714-26A>G | |
| ENST00000687278.1:c.731-26A>G | ENSP00000509593.1:n.731-26A>G | |
| ENST00000003084.11:c.3140-26A>G MANE Select | ENSP00000003084.6:n.3140-26A>G | |
| ENST00000647720.1:c.790-26A>G | ||
| ENST00000648260.1:c.1922-26A>G | ENSP00000497957.1:n.1922-26A>G | |
| ENST00000649406.1:c.2957-26A>G | ENSP00000497965.1:n.2957-26A>G | |
| ENST00000649781.1:c.2957-26A>G | ENSP00000497203.1:n.2957-26A>G | |
| ENST00000003084.10:c.3140-26A>G | ENSP00000003084.6:n.3140-26A>G | |
| ENST00000426809.5:c.3050-26A>G | ENSP00000389119.1:n.3050-26A>G | |
| NM_000492.3:c.3140-26A>G , LRG_663t1:c.3140-26A>G | NP_000483.3:n.3140-26A>G | |
| XM_011515751.1:c.3230-26A>G | XP_011514053.1:n.3230-26A>G | |
| XM_011515752.1:c.3230-26A>G | XP_011514054.1:n.3230-26A>G | |
| XM_011515753.1:c.2897-26A>G | XP_011514055.1:n.2897-26A>G | |
| XM_011515754.1:c.2897-26A>G | XP_011514056.1:n.2897-26A>G | |
| NM_000492.4:c.3140-26A>G MANE Select | NP_000483.3:n.3140-26A>G |