Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31860558C>G , CM000668.2:g.31860558C>G | GRCh38 |
| NC_000006.11:g.31828335C>G , CM000668.1:g.31828335C>G | GRCh37 |
| NC_000006.10:g.31936314C>G | NCBI36 |
| NG_008201.1:g.7375G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000375631.5:c.679G>C MANE Select | ENSP00000364782.4:p.Gly227Arg | |
| ENST00000677054.1:n.1922G>C | ||
| ENST00000677512.1:n.787G>C | ||
| ENST00000678869.1:n.1353G>C | ||
| ENST00000375631.4:c.679G>C | ENSP00000364782.4:p.Gly227Arg | |
| ENST00000480384.1:n.708G>C | ||
| ENST00000491768.5:c.679G>C | ENSP00000433127.1:p.Gly227Arg | |
| ENST00000495807.1:n.1813G>C | ||
| NM_000434.3:c.679G>C | NP_000425.1:p.Gly227Arg | |
| NM_000434.4:c.679G>C MANE Select | NP_000425.1:p.Gly227Arg |