Linked Data
dbSNP Id:
rs771036928
ExAC:
11:6340564 G / T
gnomAD v2:
11-6340564-G-T
gnomAD v4:
11-6319334-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.6319334G>T , CM000673.2:g.6319334G>T | GRCh38 |
| NC_000011.9:g.6340564G>T , CM000673.1:g.6340564G>T | GRCh37 |
| NC_000011.8:g.6297140G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303927.4:c.615C>A MANE Select | ENSP00000307292.3:p.Thr205= | |
| ENST00000303927.3:c.615C>A | ENSP00000307292.3:p.Thr205= | |
| ENST00000524852.1:n.401C>A | ||
| ENST00000530979.1:c.711C>A | ENSP00000432047.1:p.Thr237= | |
| ENST00000532354.1:n.637C>A | ||
| NM_145040.2:c.615C>A | NP_659477.2:p.Thr205= | |
| XR_930997.1:n.720+1114G>T | ||
| XR_242848.4:n.194G>T | ||
| NM_145040.3:c.615C>A MANE Select | NP_659477.2:p.Thr205= |