Linked Data
ClinVar Variation Id:
54014
dbSNP Id:
rs121908793
ExAC:
7:117175301 G / T
gnomAD v2:
7-117175301-G-T
gnomAD v4:
7-117535247-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.117535247G>T , CM000669.2:g.117535247G>T | GRCh38 |
| NC_000007.13:g.117175301G>T , CM000669.1:g.117175301G>T | GRCh37 |
| NC_000007.12:g.116962537G>T | NCBI36 |
| NG_016465.4:g.74464G>T , LRG_663:g.74464G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647720.2:c.580-1G>T | ENSP00000497673.2:n.580-1G>T | |
| ENST00000647978.2:c.*477-1G>T | ENSP00000497658.1:n.*477-1G>T | |
| ENST00000649781.2:c.580-1G>T | ENSP00000497203.1:n.580-1G>T | |
| ENST00000685018.2:c.580-1G>T | ENSP00000510194.2:n.580-1G>T | |
| ENST00000687278.2:c.580-1G>T | ENSP00000509593.2:n.580-1G>T | |
| ENST00000699585.1:c.580-1G>T | ENSP00000514456.1:n.580-1G>T | |
| ENST00000699596.1:c.580-1G>T | ENSP00000514465.1:n.580-1G>T | |
| ENST00000699597.1:c.580-1G>T | ENSP00000514466.1:n.580-1G>T | |
| ENST00000699598.1:c.580-1G>T | ENSP00000514467.1:n.580-1G>T | |
| ENST00000699599.1:c.580-1G>T | ENSP00000514468.1:n.580-1G>T | |
| ENST00000699600.1:c.580-1G>T | ENSP00000514469.1:n.580-1G>T | |
| ENST00000699601.1:c.580-1G>T | ENSP00000514470.1:n.580-1G>T | |
| ENST00000699602.1:c.580-1G>T | ENSP00000514471.1:n.580-1G>T | |
| ENST00000699604.1:c.*404-1G>T | ENSP00000514472.1:n.*404-1G>T | |
| ENST00000699605.1:c.337-1G>T | ENSP00000514473.1:n.337-1G>T | |
| ENST00000003084.11:c.580-1G>T MANE Select | ENSP00000003084.6:n.580-1G>T | |
| ENST00000647978.1:c.*477-1G>T | ENSP00000497658.1:n.*477-1G>T | |
| ENST00000648260.1:c.580-1G>T | ENSP00000497957.1:n.580-1G>T | |
| ENST00000649406.1:c.580-1G>T | ENSP00000497965.1:n.580-1G>T | |
| ENST00000649781.1:c.580-1G>T | ENSP00000497203.1:n.580-1G>T | |
| ENST00000673785.1:c.337-1G>T | ENSP00000501235.1:n.337-1G>T | |
| ENST00000003084.10:c.580-1G>T | ENSP00000003084.6:n.580-1G>T | |
| ENST00000426809.5:c.490-1G>T | ENSP00000389119.1:n.490-1G>T | |
| NM_000492.3:c.580-1G>T , LRG_663t1:c.580-1G>T | NP_000483.3:n.580-1G>T | |
| XM_011515751.1:c.670-1G>T | XP_011514053.1:n.670-1G>T | |
| XM_011515752.1:c.670-1G>T | XP_011514054.1:n.670-1G>T | |
| XM_011515753.1:c.337-1G>T | XP_011514055.1:n.337-1G>T | |
| XM_011515754.1:c.337-1G>T | XP_011514056.1:n.337-1G>T | |
| NM_000492.4:c.580-1G>T MANE Select | NP_000483.3:n.580-1G>T |