Linked Data
ClinVar Variation Id:
392192
dbSNP Id:
rs371480627
ExAC:
6:116754599 G / A
gnomAD v2:
6-116754599-G-A
gnomAD v3:
6-116433436-G-A
gnomAD v4:
6-116433436-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.116433436G>A , CM000668.2:g.116433436G>A | GRCh38 |
| NC_000006.11:g.116754599G>A , CM000668.1:g.116754599G>A | GRCh37 |
| NC_000006.10:g.116861292G>A | NCBI36 |
| NG_033266.1:g.158317G>A | |
| NG_033266.3:g.184285G>A | |
| NG_033266.4:g.184266G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000359564.3:c.911-2151G>A | ENSP00000352567.3:n.911-2151G>A | |
| ENST00000644252.3:c.1004G>A MANE Select | ENSP00000494147.2:p.Arg335His | |
| ENST00000644499.1:c.766+2243G>A | ENSP00000495266.1:n.766+2243G>A | |
| ENST00000646710.1:c.671-2151G>A | ENSP00000495970.1:n.671-2151G>A | |
| ENST00000647244.1:c.671-2151G>A | ENSP00000495184.1:n.671-2151G>A | |
| ENST00000331677.7:c.1004G>A | ENSP00000332151.2:p.Arg335His | |
| ENST00000359564.2:c.1004G>A | ENSP00000352567.2:p.Arg335His | |
| ENST00000452085.7:c.1004G>A | ENSP00000404049.2:p.Arg335His | |
| ENST00000606712.1:n.908G>A | ||
| NM_001080976.1:c.1004G>A | NP_001074445.1:p.Arg335His | |
| NM_013352.2:c.1004G>A | NP_037484.1:p.Arg335His | |
| XM_011535785.1:c.84-2151G>A | XP_011534087.1:n.84-2151G>A | |
| NM_001080976.2:c.1004G>A | NP_001074445.1:p.Arg335His | |
| NM_001322937.1:c.1004G>A | NP_001309866.1:p.Arg335His | |
| NM_001322938.1:c.1004G>A | NP_001309867.1:p.Arg335His | |
| NM_001322939.1:c.1061G>A | NP_001309868.1:p.Arg354His | |
| NM_001322940.1:c.443G>A | NP_001309869.1:p.Arg148His | |
| NM_001322941.1:c.443G>A | NP_001309870.1:p.Arg148His | |
| NM_001322943.1:c.671-2151G>A | NP_001309872.1:n.671-2151G>A | |
| NM_001322944.1:c.911-2151G>A | NP_001309873.1:n.911-2151G>A | |
| NM_013352.3:c.1004G>A | NP_037484.1:p.Arg335His | |
| NR_136524.1:n.1158-2151G>A | ||
| XM_017010795.1:c.1061G>A | XP_016866284.1:p.Arg354His | |
| XM_017010796.1:c.1004G>A | XP_016866285.1:p.Arg335His | |
| XM_017010797.1:c.968-2151G>A | XP_016866286.1:n.968-2151G>A | |
| NM_001080976.3:c.1004G>A | NP_001074445.1:p.Arg335His | |
| NM_001322937.2:c.1004G>A | NP_001309866.1:p.Arg335His | |
| NM_001322938.2:c.1004G>A | NP_001309867.1:p.Arg335His | |
| NM_001322939.2:c.1061G>A | NP_001309868.1:p.Arg354His | |
| NM_001322940.2:c.443G>A | NP_001309869.1:p.Arg148His | |
| NM_001322941.2:c.443G>A | NP_001309870.1:p.Arg148His | |
| NM_001322943.2:c.671-2151G>A | NP_001309872.1:n.671-2151G>A | |
| NM_001322944.2:c.911-2151G>A | NP_001309873.1:n.911-2151G>A | |
| NM_001374520.1:c.5G>A | NP_001361449.1:p.Arg2His | |
| NM_001374521.1:c.84-2151G>A | NP_001361450.1:n.84-2151G>A | |
| NM_013352.4:c.1004G>A MANE Select | NP_037484.1:p.Arg335His | |
| NR_136524.2:n.1135-2151G>A |