Linked Data
dbSNP Id:
rs749315555
gnomAD v2:
1-151378927-G-A
gnomAD v3:
1-151406451-G-A
gnomAD v4:
1-151406451-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.151406451G>A , CM000663.2:g.151406451G>A | GRCh38 |
| NC_000001.10:g.151378927G>A , CM000663.1:g.151378927G>A | GRCh37 |
| NC_000001.9:g.149645551G>A | NCBI36 |
| NG_046601.1:g.58015C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000710270.1:c.2632C>T | ENSP00000518163.1:p.Arg878Cys | |
| ENST00000392723.6:c.2425C>T | ENSP00000376484.1:p.Arg809Cys | |
| ENST00000439756.2:c.2584C>T | ENSP00000390156.2:p.Arg862Cys | |
| ENST00000703168.1:c.2605C>T | ENSP00000515214.1:p.Arg869Cys | |
| ENST00000271715.7:c.2584C>T MANE Select | ENSP00000271715.2:p.Arg862Cys | |
| ENST00000271715.6:c.2584C>T | ENSP00000271715.2:p.Arg862Cys | |
| ENST00000358476.7:n.2732C>T | ||
| ENST00000368863.6:c.2299C>T | ENSP00000357856.2:p.Arg767Cys | |
| ENST00000392723.5:c.2425C>T | ENSP00000376484.1:p.Arg809Cys | |
| ENST00000409503.5:c.2557C>T | ENSP00000386836.1:p.Arg853Cys | |
| ENST00000491586.5:c.2452C>T | ENSP00000418408.1:p.Arg818Cys | |
| ENST00000529669.1:c.784C>T | ENSP00000432295.1:p.Arg262Cys | |
| ENST00000531094.5:c.2398C>T | ENSP00000431259.1:p.Arg800Cys | |
| NM_001194937.1:c.2557C>T | NP_001181866.1:p.Arg853Cys | |
| NM_001194938.1:c.2398C>T | NP_001181867.1:p.Arg800Cys | |
| NM_015100.3:c.2584C>T | NP_055915.2:p.Arg862Cys | |
| NM_145796.3:c.2299C>T | NP_665739.3:p.Arg767Cys | |
| NM_207171.2:c.2425C>T | NP_997054.1:p.Arg809Cys | |
| XM_005244999.1:c.2584C>T | XP_005245056.1:p.Arg862Cys | |
| XM_005245000.3:c.2584C>T | XP_005245057.1:p.Arg862Cys | |
| XM_005245001.1:c.2584C>T | XP_005245058.1:p.Arg862Cys | |
| XM_005245005.1:c.2425C>T | XP_005245062.1:p.Arg809Cys | |
| XM_005245006.3:c.2425C>T | XP_005245063.1:p.Arg809Cys | |
| XM_011509330.1:c.2476C>T | XP_011507632.1:p.Arg826Cys | |
| XM_011509331.1:c.2227C>T | XP_011507633.1:p.Arg743Cys | |
| XR_921760.1:n.2412C>T | ||
| XM_005244999.3:c.2584C>T | XP_005245056.1:p.Arg862Cys | |
| XM_005245000.4:c.2584C>T | XP_005245057.1:p.Arg862Cys | |
| XM_005245001.2:c.2584C>T | XP_005245058.1:p.Arg862Cys | |
| XM_005245005.2:c.2425C>T | XP_005245062.1:p.Arg809Cys | |
| XM_005245006.5:c.2425C>T | XP_005245063.1:p.Arg809Cys | |
| XM_017000744.1:c.2605C>T | XP_016856233.1:p.Arg869Cys | |
| XM_017000745.2:c.2557C>T | XP_016856234.1:p.Arg853Cys | |
| XM_017000746.1:c.2557C>T | XP_016856235.1:p.Arg853Cys | |
| XM_017000748.1:c.2425C>T | XP_016856237.1:p.Arg809Cys | |
| XM_017000749.1:c.2425C>T | XP_016856238.1:p.Arg809Cys | |
| XM_024454305.1:c.2458C>T | XP_024310073.1:p.Arg820Cys | |
| XM_024454306.1:c.1384C>T | XP_024310074.1:p.Arg462Cys | |
| XR_002959801.1:n.2439C>T | ||
| NM_015100.4:c.2584C>T MANE Select | NP_055915.2:p.Arg862Cys | |
| NM_001194937.2:c.2557C>T | NP_001181866.1:p.Arg853Cys | |
| NM_001194938.2:c.2398C>T | NP_001181867.1:p.Arg800Cys | |
| NM_145796.4:c.2299C>T | NP_665739.3:p.Arg767Cys |