Linked Data
dbSNP Id:
rs75028895
ExAC:
1:17672519 C / G
gnomAD v2:
1-17672519-C-G
gnomAD v3:
1-17346024-C-G
gnomAD v4:
1-17346024-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.17346024C>G , CM000663.2:g.17346024C>G | GRCh38 |
| NC_000001.10:g.17672519C>G , CM000663.1:g.17672519C>G | GRCh37 |
| NC_000001.9:g.17545106C>G | NCBI36 |
| NG_023261.2:g.42835C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375448.4:c.936-4C>G MANE Select | ENSP00000364597.4:n.936-4C>G | |
| NM_012387.2:c.936-4C>G | NP_036519.2:n.936-4C>G | |
| XM_011541150.1:c.750-4C>G | XP_011539452.1:n.750-4C>G | |
| XM_011541151.1:c.936-4C>G | XP_011539453.1:n.936-4C>G | |
| XM_011541152.1:c.399-4C>G | XP_011539454.1:n.399-4C>G | |
| XM_011541153.1:c.936-4C>G | XP_011539455.1:n.936-4C>G | |
| XM_011541154.1:c.936-4C>G | XP_011539456.1:n.936-4C>G | |
| XM_011541155.1:c.936-4C>G | XP_011539457.1:n.936-4C>G | |
| XM_011541156.1:c.936-4C>G | XP_011539458.1:n.936-4C>G | |
| XM_011541157.1:c.45-4C>G | XP_011539459.1:n.45-4C>G | |
| XM_011541154.2:c.936-4C>G | XP_011539456.1:n.936-4C>G | |
| NM_012387.3:c.936-4C>G MANE Select | NP_036519.2:n.936-4C>G |