Linked Data
dbSNP Id:
rs1051296
ExAC:
21:46934861 A / C
gnomAD v2:
21-46934861-A-C
gnomAD v3:
21-45514947-A-C
gnomAD v4:
21-45514947-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.45514947A>C , CM000683.2:g.45514947A>C | GRCh38 |
| NC_000021.8:g.46934861A>C , CM000683.1:g.46934861A>C | GRCh37 |
| NC_000021.7:g.45759289A>C | NCBI36 |
| NG_011903.1:g.114756A>C | |
| NG_028278.1:g.32525T>G | |
| NG_028278.2:g.53197T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000311124.9:c.*711T>G MANE Select | ENSP00000308895.4:n.*711T>G | |
| ENST00000650808.1:c.*29T>G | ENSP00000498221.1:n.*29T>G | |
| ENST00000311124.8:c.*711T>G | ENSP00000308895.4:n.*711T>G | |
| ENST00000380010.8:c.*29T>G | ENSP00000369347.4:n.*29T>G | |
| ENST00000417954.5:c.497+10870T>G | ||
| ENST00000460174.1:n.335T>G | ||
| ENST00000468508.1:n.187T>G | ||
| ENST00000567670.5:c.1293+10870T>G | ENSP00000457278.1:n.1293+10870T>G | |
| NM_001205206.1:c.*29T>G | NP_001192135.1:n.*29T>G | |
| NM_001205207.1:c.*711T>G | NP_001192136.1:n.*711T>G | |
| NM_194255.2:c.*711T>G | NP_919231.1:n.*711T>G | |
| XM_005261164.2:c.*711T>G | XP_005261221.1:n.*711T>G | |
| XM_011529696.1:c.*711T>G | XP_011527998.1:n.*711T>G | |
| XM_011529697.1:c.*711T>G | XP_011527999.1:n.*711T>G | |
| XM_011529698.1:c.*711T>G | XP_011528000.1:n.*711T>G | |
| XM_011529699.1:c.*711T>G | XP_011528001.1:n.*711T>G | |
| XM_011529700.1:c.*711T>G | XP_011528002.1:n.*711T>G | |
| XM_011529701.1:c.*711T>G | XP_011528003.1:n.*711T>G | |
| XM_011529702.1:c.*711T>G | XP_011528004.1:n.*711T>G | |
| XM_011529703.1:c.*711T>G | XP_011528005.1:n.*711T>G | |
| XM_011529704.1:c.*711T>G | XP_011528006.1:n.*711T>G | |
| XM_011529705.1:c.*29T>G | XP_011528007.1:n.*29T>G | |
| XM_011529706.1:c.*711T>G | XP_011528008.1:n.*711T>G | |
| XM_011529707.1:c.1584+10870T>G | XP_011528009.1:n.1584+10870T>G | |
| XM_011529708.1:c.*711T>G | XP_011528010.1:n.*711T>G | |
| XM_011529709.1:c.*711T>G | XP_011528011.1:n.*711T>G | |
| XM_011529710.1:c.*711T>G | XP_011528012.1:n.*711T>G | |
| NM_001205206.2:c.*29T>G | NP_001192135.1:n.*29T>G | |
| NM_001205207.2:c.*711T>G | NP_001192136.1:n.*711T>G | |
| NM_001352510.1:c.*711T>G | NP_001339439.1:n.*711T>G | |
| NM_001352511.1:c.*29T>G | NP_001339440.1:n.*29T>G | |
| NM_001352512.1:c.*711T>G | NP_001339441.1:n.*711T>G | |
| NM_194255.3:c.*711T>G | NP_919231.1:n.*711T>G | |
| XM_011529696.2:c.*711T>G | XP_011527998.1:n.*711T>G | |
| XM_011529698.2:c.*711T>G | XP_011528000.1:n.*711T>G | |
| XM_011529700.2:c.*711T>G | XP_011528002.1:n.*711T>G | |
| XM_011529701.2:c.*711T>G | XP_011528003.1:n.*711T>G | |
| XM_011529702.2:c.*711T>G | XP_011528004.1:n.*711T>G | |
| XM_011529703.2:c.*711T>G | XP_011528005.1:n.*711T>G | |
| XM_011529706.3:c.*711T>G | XP_011528008.1:n.*711T>G | |
| XM_011529709.2:c.*711T>G | XP_011528011.1:n.*711T>G | |
| XM_017028443.1:c.*711T>G | XP_016883932.1:n.*711T>G | |
| XM_017028444.1:c.*29T>G | XP_016883933.1:n.*29T>G | |
| XM_017028445.2:c.1584+10870T>G | XP_016883934.1:n.1584+10870T>G | |
| NM_194255.4:c.*711T>G MANE Select | NP_919231.1:n.*711T>G | |
| NM_001205206.3:c.*29T>G | NP_001192135.1:n.*29T>G | |
| NM_001205207.3:c.*711T>G | NP_001192136.1:n.*711T>G | |
| NM_001352510.2:c.*711T>G | NP_001339439.1:n.*711T>G | |
| NM_001352511.2:c.*29T>G | NP_001339440.1:n.*29T>G | |
| NM_001352512.2:c.*711T>G | NP_001339441.1:n.*711T>G | |
| NM_001205206.4:c.*29T>G | NP_001192135.1:n.*29T>G | |
| NM_001352511.3:c.*29T>G | NP_001339440.1:n.*29T>G |