Linked Data
dbSNP Id:
rs188222189
gnomAD v2:
3-3055406-C-G
gnomAD v3:
3-3013722-C-G
gnomAD v4:
3-3013722-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.3013722C>G , CM000665.2:g.3013722C>G | GRCh38 |
| NC_000003.11:g.3055406C>G , CM000665.1:g.3055406C>G | GRCh37 |
| NC_000003.10:g.3030406C>G | NCBI36 |
| NG_012827.1:g.918160C>G | |
| NG_012827.2:g.918160C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000418658.6:c.1487-12380C>G MANE Select | ENSP00000396010.1:n.1487-12380C>G | |
| ENST00000397459.6:c.503-12380C>G | ENSP00000380600.2:n.503-12380C>G | |
| ENST00000397461.5:c.1487-12380C>G | ENSP00000380602.1:n.1487-12380C>G | |
| ENST00000418658.5:c.1487-12380C>G | ENSP00000396010.1:n.1487-12380C>G | |
| ENST00000427331.5:c.1487-12380C>G | ENSP00000413642.1:n.1487-12380C>G | |
| ENST00000427741.5:c.*685-12380C>G | ENSP00000396719.1:n.*685-12380C>G | |
| ENST00000430505.6:n.1684-12380C>G | ||
| NM_001206955.1:c.1487-12380C>G | NP_001193884.1:n.1487-12380C>G | |
| NM_001206956.1:c.503-12380C>G | NP_001193885.1:n.503-12380C>G | |
| NM_175607.2:c.1487-12380C>G | NP_783200.1:n.1487-12380C>G | |
| NM_175613.2:c.503-12380C>G | NP_783302.1:n.503-12380C>G | |
| XM_006713004.2:c.1487-12380C>G | XP_006713067.1:n.1487-12380C>G | |
| XM_011533425.1:c.1487-12380C>G | XP_011531727.1:n.1487-12380C>G | |
| XM_011533426.1:c.1487-12380C>G | XP_011531728.1:n.1487-12380C>G | |
| XM_011533427.1:c.1487-12380C>G | XP_011531729.1:n.1487-12380C>G | |
| XM_011533428.1:c.1487-12380C>G | XP_011531730.1:n.1487-12380C>G | |
| XM_011533429.1:c.1487-12380C>G | XP_011531731.1:n.1487-12380C>G | |
| XM_011533430.1:c.1487-12380C>G | XP_011531732.1:n.1487-12380C>G | |
| XM_011533431.1:c.1454-12380C>G | XP_011531733.1:n.1454-12380C>G | |
| NM_001350095.1:c.1487-12380C>G | NP_001337024.1:n.1487-12380C>G | |
| XM_006713004.4:c.1487-12380C>G | XP_006713067.1:n.1487-12380C>G | |
| XM_011533425.3:c.1487-12380C>G | XP_011531727.1:n.1487-12380C>G | |
| XM_011533427.2:c.1487-12380C>G | XP_011531729.1:n.1487-12380C>G | |
| XM_011533428.2:c.1487-12380C>G | XP_011531730.1:n.1487-12380C>G | |
| XM_011533429.2:c.1487-12380C>G | XP_011531731.1:n.1487-12380C>G | |
| XM_011533430.2:c.1487-12380C>G | XP_011531732.1:n.1487-12380C>G | |
| XM_011533431.2:c.1454-12380C>G | XP_011531733.1:n.1454-12380C>G | |
| XM_017005782.1:c.1487-12380C>G | XP_016861271.1:n.1487-12380C>G | |
| XM_017005783.1:c.1487-12380C>G | XP_016861272.1:n.1487-12380C>G | |
| XM_017005784.2:c.1487-12380C>G | XP_016861273.1:n.1487-12380C>G | |
| XM_017005785.1:c.1487-12380C>G | XP_016861274.1:n.1487-12380C>G | |
| XM_017005786.1:c.1487-12380C>G | XP_016861275.1:n.1487-12380C>G | |
| XM_017005787.1:c.1487-12380C>G | XP_016861276.1:n.1487-12380C>G | |
| NM_175607.3:c.1487-12380C>G MANE Select | NP_783200.1:n.1487-12380C>G | |
| NM_001206955.2:c.1487-12380C>G | NP_001193884.1:n.1487-12380C>G | |
| NM_001206956.2:c.503-12380C>G | NP_001193885.1:n.503-12380C>G | |
| NM_001350095.2:c.1487-12380C>G | NP_001337024.1:n.1487-12380C>G | |
| NM_175613.3:c.503-12380C>G | NP_783302.1:n.503-12380C>G |