Linked Data
ClinVar Variation Id:
7182
ClinVar RCV Id:
RCV000007602
RCV000224726
RCV000508504
RCV001027909
RCV001009366
RCV001004250
RCV003473034
dbSNP Id:
rs77932196
ExAC:
7:117180324 G / A
gnomAD v2:
7-117180324-G-A
gnomAD v3:
7-117540270-G-A
gnomAD v4:
7-117540270-G-A
COSMIC:
COSM1673484
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.117540270G>A , CM000669.2:g.117540270G>A | GRCh38 |
| NC_000007.13:g.117180324G>A , CM000669.1:g.117180324G>A | GRCh37 |
| NC_000007.12:g.116967560G>A | NCBI36 |
| NG_016465.4:g.79487G>A , LRG_663:g.79487G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647720.2:c.1040G>A | ENSP00000497673.2:p.Arg347His | |
| ENST00000647978.2:c.*937G>A | ENSP00000497658.1:n.*937G>A | |
| ENST00000649781.2:c.1040G>A | ENSP00000497203.1:p.Arg347His | |
| ENST00000685018.2:c.1040G>A | ENSP00000510194.2:p.Arg347His | |
| ENST00000687278.2:c.1040G>A | ENSP00000509593.2:p.Arg347His | |
| ENST00000699585.1:c.1040G>A | ENSP00000514456.1:p.Arg347His | |
| ENST00000699596.1:c.1040G>A | ENSP00000514465.1:p.Arg347His | |
| ENST00000699597.1:c.1040G>A | ENSP00000514466.1:p.Arg347His | |
| ENST00000699598.1:c.1040G>A | ENSP00000514467.1:p.Arg347His | |
| ENST00000699599.1:c.1040G>A | ENSP00000514468.1:p.Arg347His | |
| ENST00000699600.1:c.1040G>A | ENSP00000514469.1:p.Arg347His | |
| ENST00000699601.1:c.1040G>A | ENSP00000514470.1:p.Arg347His | |
| ENST00000699602.1:c.1040G>A | ENSP00000514471.1:p.Arg347His | |
| ENST00000699604.1:c.*864G>A | ENSP00000514472.1:n.*864G>A | |
| ENST00000699605.1:c.797G>A | ENSP00000514473.1:p.Arg266His | |
| ENST00000003084.11:c.1040G>A MANE Select | ENSP00000003084.6:p.Arg347His | |
| ENST00000647978.1:c.*937G>A | ENSP00000497658.1:n.*937G>A | |
| ENST00000648260.1:c.1040G>A | ENSP00000497957.1:p.Arg347His | |
| ENST00000649406.1:c.1040G>A | ENSP00000497965.1:p.Arg347His | |
| ENST00000649781.1:c.1040G>A | ENSP00000497203.1:p.Arg347His | |
| ENST00000673785.1:c.797G>A | ENSP00000501235.1:p.Arg266His | |
| ENST00000003084.10:c.1040G>A | ENSP00000003084.6:p.Arg347His | |
| ENST00000426809.5:c.950G>A | ENSP00000389119.1:p.Arg317His | |
| NM_000492.3:c.1040G>A , LRG_663t1:c.1040G>A | NP_000483.3:p.Arg347His | |
| XM_011515751.1:c.1130G>A | XP_011514053.1:p.Arg377His | |
| XM_011515752.1:c.1130G>A | XP_011514054.1:p.Arg377His | |
| XM_011515753.1:c.797G>A | XP_011514055.1:p.Arg266His | |
| XM_011515754.1:c.797G>A | XP_011514056.1:p.Arg266His | |
| NM_000492.4:c.1040G>A MANE Select | NP_000483.3:p.Arg347His |