Linked Data
dbSNP Id:
rs750971577
ExAC:
1:236925927 C / T
gnomAD v2:
1-236925927-C-T
gnomAD v4:
1-236762627-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.236762627C>T , CM000663.2:g.236762627C>T | GRCh38 |
| NC_000001.10:g.236925927C>T , CM000663.1:g.236925927C>T | GRCh37 |
| NC_000001.9:g.234992550C>T | NCBI36 |
| NG_009081.1:g.81158C>T | |
| NG_009081.2:g.103487C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000542672.7:c.*8C>T | ENSP00000443495.1:n.*8C>T | |
| ENST00000461367.2:n.989C>T | ||
| ENST00000492634.7:n.2623C>T | ||
| ENST00000682015.1:c.*8C>T | ENSP00000506961.1:n.*8C>T | |
| ENST00000682490.1:n.611C>T | ||
| ENST00000682692.1:n.3788C>T | ||
| ENST00000682966.1:n.8334C>T | ||
| ENST00000683111.1:c.*1979C>T | ENSP00000507913.1:n.*1979C>T | |
| ENST00000683322.1:n.4045C>T | ||
| ENST00000683805.1:n.1484C>T | ||
| ENST00000684050.1:n.5331C>T | ||
| ENST00000684122.1:n.2127C>T | ||
| ENST00000684286.1:n.4248C>T | ||
| ENST00000684502.1:n.3990C>T | ||
| ENST00000684763.1:n.1308C>T | ||
| ENST00000366578.6:c.*8C>T MANE Select | ENSP00000355537.4:n.*8C>T | |
| ENST00000492634.6:n.2623C>T | ||
| ENST00000542672.6:c.*8C>T | ENSP00000443495.1:n.*8C>T | |
| ENST00000651275.1:c.2585C>T | ENSP00000498926.1:n.2585C>T | |
| ENST00000651781.1:c.1773C>T | ||
| ENST00000651786.1:c.*2065C>T | ENSP00000498364.1:n.*2065C>T | |
| ENST00000652096.1:c.*2098C>T | ENSP00000498896.1:n.*2098C>T | |
| ENST00000366578.5:c.*8C>T | ENSP00000355537.4:n.*8C>T | |
| ENST00000542672.5:c.*8C>T | ENSP00000443495.1:n.*8C>T | |
| ENST00000546208.5:c.*8C>T | ENSP00000438384.2:n.*8C>T | |
| NM_001103.3:c.*8C>T | NP_001094.1:n.*8C>T | |
| NM_001278343.1:c.*8C>T | NP_001265272.1:n.*8C>T | |
| NM_001278344.1:c.*8C>T | NP_001265273.1:n.*8C>T | |
| NM_001278343.2:c.*8C>T | NP_001265272.1:n.*8C>T | |
| NM_001103.4:c.*8C>T MANE Select | NP_001094.1:n.*8C>T | |
| NM_001278344.2:c.*8C>T | NP_001265273.1:n.*8C>T |