Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31861366A>C , CM000668.2:g.31861366A>C | GRCh38 |
| NC_000006.11:g.31829143A>C , CM000668.1:g.31829143A>C | GRCh37 |
| NC_000006.10:g.31937122A>C | NCBI36 |
| NG_008201.1:g.6567T>G | |
| NG_023058.1:g.22681T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375631.5:c.437T>G MANE Select | ENSP00000364782.4:p.Val146Gly | |
| ENST00000677054.1:n.1114T>G | ||
| ENST00000677512.1:n.545T>G | ||
| ENST00000678869.1:n.545T>G | ||
| ENST00000375631.4:c.437T>G | ENSP00000364782.4:p.Val146Gly | |
| ENST00000480384.1:n.466T>G | ||
| ENST00000491768.5:c.437T>G | ENSP00000433127.1:p.Val146Gly | |
| ENST00000495807.1:n.1005T>G | ||
| NM_000434.3:c.437T>G | NP_000425.1:p.Val146Gly | |
| NM_000434.4:c.437T>G MANE Select | NP_000425.1:p.Val146Gly |