Linked Data
dbSNP Id:
rs770381751
ExAC:
11:66328028 T / C
gnomAD v2:
11-66328028-T-C
gnomAD v4:
11-66560557-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.66560557T>C , CM000673.2:g.66560557T>C | GRCh38 |
| NC_000011.9:g.66328028T>C , CM000673.1:g.66328028T>C | GRCh37 |
| NC_000011.8:g.66084604T>C | NCBI36 |
| NG_013304.2:g.18638T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000513398.2:c.1678-16T>C MANE Select | ENSP00000426797.1:n.1678-16T>C | |
| ENST00000502692.5:c.1807-16T>C | ENSP00000422007.1:n.1807-16T>C | |
| ENST00000513398.1:c.1678-16T>C | ENSP00000426797.1:n.1678-16T>C | |
| NM_001104.3:c.1678-16T>C | NP_001095.2:n.1678-16T>C | |
| NM_001258371.2:c.1807-16T>C | NP_001245300.2:n.1807-16T>C | |
| NM_001104.4:c.1678-16T>C MANE Select | NP_001095.2:n.1678-16T>C | |
| NM_001258371.3:c.1807-16T>C | NP_001245300.2:n.1807-16T>C |