Linked Data
ClinVar Variation Id:
283982
dbSNP Id:
rs886042758
gnomAD v3:
2-71682605-G-T
gnomAD v4:
2-71682605-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.71682605G>T , CM000664.2:g.71682605G>T | GRCh38 |
| NC_000002.11:g.71909735G>T , CM000664.1:g.71909735G>T | GRCh37 |
| NC_000002.10:g.71763243G>T | NCBI36 |
| NG_008694.1:g.233983G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000698057.1:c.3663G>T | ENSP00000513536.1:p.Arg1221= | |
| ENST00000698058.1:c.2880G>T | ENSP00000513537.1:p.Arg960= | |
| ENST00000698059.1:c.2988G>T | ENSP00000513538.1:p.Arg996= | |
| ENST00000258104.8:c.6132G>T MANE Plus Clinical | ENSP00000258104.3:p.Arg2044= | |
| ENST00000410020.8:c.6249G>T MANE Select | ENSP00000386881.3:p.Arg2083= | |
| ENST00000258104.7:c.6132G>T | ENSP00000258104.3:p.Arg2044= | |
| ENST00000394120.6:c.6135G>T | ENSP00000377678.2:p.Arg2045= | |
| ENST00000409366.5:c.6198G>T | ENSP00000386512.1:p.Arg2066= | |
| ENST00000409582.7:c.6246G>T | ENSP00000386547.3:p.Arg2082= | |
| ENST00000409651.5:c.6228G>T | ENSP00000386683.1:p.Arg2076= | |
| ENST00000409744.5:c.6156G>T | ENSP00000386285.1:p.Arg2052= | |
| ENST00000409762.5:c.6183G>T | ENSP00000387137.1:p.Arg2061= | |
| ENST00000410020.7:c.6249G>T | ENSP00000386881.3:p.Arg2083= | |
| ENST00000410041.1:c.6186G>T | ENSP00000386617.1:p.Arg2062= | |
| ENST00000413539.6:c.6225G>T | ENSP00000407046.2:p.Arg2075= | |
| ENST00000429174.6:c.6195G>T | ENSP00000398305.2:p.Arg2065= | |
| ENST00000479049.6:n.3017G>T | ||
| NM_001130455.1:c.6135G>T | NP_001123927.1:p.Arg2045= | |
| NM_001130976.1:c.6090G>T | NP_001124448.1:p.Arg2030= | |
| NM_001130977.1:c.6153G>T | NP_001124449.1:p.Arg2051= | |
| NM_001130978.1:c.6195G>T | NP_001124450.1:p.Arg2065= | |
| NM_001130979.1:c.6225G>T | NP_001124451.1:p.Arg2075= | |
| NM_001130980.1:c.6183G>T | NP_001124452.1:p.Arg2061= | |
| NM_001130981.1:c.6246G>T | NP_001124453.1:p.Arg2082= | |
| NM_001130982.1:c.6228G>T | NP_001124454.1:p.Arg2076= | |
| NM_001130983.1:c.6198G>T | NP_001124455.1:p.Arg2066= | |
| NM_001130984.1:c.6156G>T | NP_001124456.1:p.Arg2052= | |
| NM_001130985.1:c.6186G>T | NP_001124457.1:p.Arg2062= | |
| NM_001130986.1:c.6093G>T | NP_001124458.1:p.Arg2031= | |
| NM_001130987.1:c.6249G>T | NP_001124459.1:p.Arg2083= | |
| NM_003494.3:c.6132G>T | NP_003485.1:p.Arg2044= | |
| XM_005264584.3:c.6291G>T | XP_005264641.1:p.Arg2097= | |
| XM_005264585.3:c.6288G>T | XP_005264642.1:p.Arg2096= | |
| XM_005264584.4:c.6291G>T | XP_005264641.1:p.Arg2097= | |
| XM_005264585.5:c.6288G>T | XP_005264642.1:p.Arg2096= | |
| NM_001130987.2:c.6249G>T MANE Select | NP_001124459.1:p.Arg2083= | |
| NM_001130455.2:c.6135G>T | NP_001123927.1:p.Arg2045= | |
| NM_001130976.2:c.6090G>T | NP_001124448.1:p.Arg2030= | |
| NM_001130977.2:c.6153G>T | NP_001124449.1:p.Arg2051= | |
| NM_001130978.2:c.6195G>T | NP_001124450.1:p.Arg2065= | |
| NM_001130979.2:c.6225G>T | NP_001124451.1:p.Arg2075= | |
| NM_001130980.2:c.6183G>T | NP_001124452.1:p.Arg2061= | |
| NM_001130981.2:c.6246G>T | NP_001124453.1:p.Arg2082= | |
| NM_001130982.2:c.6228G>T | NP_001124454.1:p.Arg2076= | |
| NM_001130983.2:c.6198G>T | NP_001124455.1:p.Arg2066= | |
| NM_001130984.2:c.6156G>T | NP_001124456.1:p.Arg2052= | |
| NM_001130985.2:c.6186G>T | NP_001124457.1:p.Arg2062= | |
| NM_001130986.2:c.6093G>T | NP_001124458.1:p.Arg2031= | |
| NM_003494.4:c.6132G>T MANE Plus Clinical | NP_003485.1:p.Arg2044= |