Linked Data
dbSNP Id:
rs368907397
ExAC:
1:153963554 G / C
gnomAD v2:
1-153963554-G-C
gnomAD v4:
1-153991078-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.153991078G>C , CM000663.2:g.153991078G>C | GRCh38 |
| NC_000001.10:g.153963554G>C , CM000663.1:g.153963554G>C | GRCh37 |
| NC_000001.9:g.152230178G>C | NCBI36 |
| NG_053102.2:g.5324G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000477151.2:n.158G>C | ||
| ENST00000643794.1:c.128-37G>C | ENSP00000495765.1:n.128-37G>C | |
| ENST00000651669.1:c.7-37G>C MANE Select | ENSP00000499044.1:n.7-37G>C | |
| ENST00000368567.4:c.7-37G>C | ENSP00000357555.4:n.7-37G>C | |
| ENST00000392558.4:c.7-37G>C | ENSP00000376341.4:n.7-37G>C | |
| ENST00000477151.1:n.162-37G>C | ||
| ENST00000493224.5:n.273-37G>C | ||
| NM_001030.4:c.7-37G>C | NP_001021.1:n.7-37G>C | |
| NM_001030.6:c.7-37G>C MANE Select | NP_001021.1:n.7-37G>C | |
| NM_001349946.1:c.-90-37G>C | NP_001336875.1:n.-90-37G>C | |
| NM_001349947.1:c.-90-37G>C | NP_001336876.1:n.-90-37G>C | |
| NM_001349946.2:c.-90-37G>C | NP_001336875.1:n.-90-37G>C | |
| NM_001349947.2:c.-90-37G>C | NP_001336876.1:n.-90-37G>C |