Linked Data
dbSNP Id:
rs924281186
gnomAD v2:
3-184073493-T-C
gnomAD v3:
3-184355705-T-C
gnomAD v4:
3-184355705-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.184355705T>C , CM000665.2:g.184355705T>C | GRCh38 |
| NC_000003.11:g.184073493T>C , CM000665.1:g.184073493T>C | GRCh37 |
| NC_000003.10:g.185556187T>C | NCBI36 |
| NG_016422.1:g.10899A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265593.9:c.1159A>G (CLCN2) MANE Select | ENSP00000265593.4:p.Met387Val | |
| ENST00000475279.2:c.541A>G (CLCN2) | ||
| ENST00000636180.1:c.*135A>G (CLCN2) | ENSP00000490374.1:n.*135A>G | |
| ENST00000636241.1:c.1050A>G (CLCN2) | ||
| ENST00000636492.1:c.1042A>G (CLCN2) | ENSP00000490313.1:p.Met348Val | |
| ENST00000636658.1:c.420A>G (CLCN2) | ||
| ENST00000636661.1:c.*1349A>G (CLCN2) | ENSP00000490764.1:n.*1349A>G | |
| ENST00000637392.1:n.2271A>G (CLCN2) | ||
| ENST00000637538.1:c.465A>G (CLCN2) | ||
| ENST00000637909.1:c.965A>G (CLCN2) | ||
| ENST00000638134.1:c.967A>G (CLCN2) | ||
| ENST00000265593.8:c.1159A>G (CLCN2) | ENSP00000265593.4:p.Met387Val | |
| ENST00000344937.11:c.1159A>G (CLCN2) | ENSP00000345056.7:p.Met387Val | |
| ENST00000430397.5:c.102A>G (CLCN2) | ||
| ENST00000434054.6:c.1027A>G (CLCN2) | ENSP00000400425.2:p.Met343Val | |
| ENST00000444495.1:c.2106+210998T>C (EIF2B5) | ENSP00000409142.1:n.2106+210998T>C | |
| ENST00000457512.1:c.1159A>G (CLCN2) | ENSP00000391928.1:p.Met387Val | |
| ENST00000475279.1:n.177A>G (CLCN2) | ||
| ENST00000485667.1:n.1166A>G (CLCN2) | ||
| NM_001171087.2:c.1159A>G (CLCN2) | NP_001164558.1:p.Met387Val | |
| NM_001171088.2:c.1027A>G (CLCN2) | NP_001164559.1:p.Met343Val | |
| NM_001171089.2:c.1159A>G (CLCN2) | NP_001164560.1:p.Met387Val | |
| NM_004366.5:c.1159A>G (CLCN2) | NP_004357.3:p.Met387Val | |
| XM_006713489.1:c.1159A>G (CLCN2) | XP_006713552.1:p.Met387Val | |
| XM_006713490.1:c.1A>G (CLCN2) | XP_006713553.1:p.Met1Val | |
| XM_011512401.1:c.1159A>G (CLCN2) | XP_011510703.1:p.Met387Val | |
| XM_011512402.1:c.1159A>G (CLCN2) | XP_011510704.1:p.Met387Val | |
| XM_006713490.2:c.1A>G (CLCN2) | XP_006713553.1:p.Met1Val | |
| XR_001740001.1:n.1283A>G (CLCN2) | ||
| XR_001740002.1:n.1283A>G (CLCN2) | ||
| NM_004366.6:c.1159A>G (CLCN2) MANE Select | NP_004357.3:p.Met387Val | |
| NM_001171087.3:c.1159A>G (CLCN2) | NP_001164558.1:p.Met387Val | |
| NM_001171088.3:c.1027A>G (CLCN2) | NP_001164559.1:p.Met343Val | |
| NM_001171089.3:c.1159A>G (CLCN2) | NP_001164560.1:p.Met387Val |