Linked Data
ClinVar Variation Id:
336769
dbSNP Id:
rs201607698
ExAC:
2:63714570 A / G
gnomAD v2:
2-63714570-A-G
gnomAD v3:
2-63487436-A-G
gnomAD v4:
2-63487436-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.63487436A>G , CM000664.2:g.63487436A>G | GRCh38 |
| NC_000002.11:g.63714570A>G , CM000664.1:g.63714570A>G | GRCh37 |
| NC_000002.10:g.63568074A>G | NCBI36 |
| NG_028144.1:g.106298T>C | |
| NG_028144.2:g.358390T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000272321.12:c.208+11T>C MANE Select | ENSP00000272321.7:n.208+11T>C | |
| ENST00000272321.11:c.208+11T>C | ENSP00000272321.7:n.208+11T>C | |
| ENST00000409562.7:c.208+11T>C | ENSP00000387222.3:n.208+11T>C | |
| ENST00000409835.5:n.455+11T>C | ||
| ENST00000417238.5:c.*319+11T>C | ENSP00000411429.1:n.*319+11T>C | |
| ENST00000418148.5:c.203+11T>C | ||
| ENST00000431065.1:c.208+11T>C | ENSP00000396226.1:n.208+11T>C | |
| ENST00000490935.5:n.716+11T>C | ||
| NM_015910.5:c.208+11T>C | NP_056994.3:n.208+11T>C | |
| XM_005264348.2:c.208+11T>C | XP_005264405.1:n.208+11T>C | |
| XM_011532881.1:c.136+11T>C | XP_011531183.1:n.136+11T>C | |
| XM_011532882.1:c.109+11T>C | XP_011531184.1:n.109+11T>C | |
| XM_011532883.1:c.208+11T>C | XP_011531185.1:n.208+11T>C | |
| XM_011532884.1:c.208+11T>C | XP_011531186.1:n.208+11T>C | |
| XM_011532885.1:c.208+11T>C | XP_011531187.1:n.208+11T>C | |
| XM_011532886.1:c.208+11T>C | XP_011531188.1:n.208+11T>C | |
| XM_011532887.1:c.208+11T>C | XP_011531189.1:n.208+11T>C | |
| XM_011532888.1:c.208+11T>C | XP_011531190.1:n.208+11T>C | |
| XM_011532889.1:c.208+11T>C | XP_011531191.1:n.208+11T>C | |
| XM_011532890.1:c.208+11T>C | XP_011531192.1:n.208+11T>C | |
| XM_011532891.1:c.136+11T>C | XP_011531193.1:n.136+11T>C | |
| XR_244934.1:n.455+11T>C | ||
| XR_244935.1:n.455+11T>C | ||
| XR_939686.1:n.455+11T>C | ||
| NM_001354044.1:c.136+11T>C | NP_001340973.1:n.136+11T>C | |
| NM_001354045.1:c.208+11T>C | NP_001340974.1:n.208+11T>C | |
| NM_015910.6:c.208+11T>C | NP_056994.3:n.208+11T>C | |
| NR_148704.1:n.988+11T>C | ||
| NR_148705.1:n.736+11T>C | ||
| XM_005264348.4:c.208+11T>C | XP_005264405.1:n.208+11T>C | |
| XM_011532881.3:c.136+11T>C | XP_011531183.1:n.136+11T>C | |
| XM_011532884.3:c.208+11T>C | XP_011531186.1:n.208+11T>C | |
| XM_011532887.3:c.208+11T>C | XP_011531189.1:n.208+11T>C | |
| XM_011532890.3:c.208+11T>C | XP_011531192.1:n.208+11T>C | |
| XM_011532891.2:c.136+11T>C | XP_011531193.1:n.136+11T>C | |
| XM_017004253.2:c.208+11T>C | XP_016859742.1:n.208+11T>C | |
| XM_017004254.2:c.208+11T>C | XP_016859743.1:n.208+11T>C | |
| XR_001738759.2:n.670+11T>C | ||
| XR_001738760.2:n.670+11T>C | ||
| XR_002959303.1:n.670+11T>C | ||
| XR_244934.3:n.670+11T>C | ||
| NM_015910.7:c.208+11T>C MANE Select | NP_056994.3:n.208+11T>C | |
| NM_001354044.2:c.136+11T>C | NP_001340973.1:n.136+11T>C | |
| NM_001354045.2:c.208+11T>C | NP_001340974.1:n.208+11T>C | |
| NR_148704.2:n.666+11T>C | ||
| NR_148705.2:n.414+11T>C |