Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31861397C= , CM000668.2:g.31861397C= | GRCh38 |
| NC_000006.11:g.31829174C= , CM000668.1:g.31829174C= | GRCh37 |
| NC_000006.10:g.31937153C= | NCBI36 |
| NG_008201.1:g.6536G= | |
| NG_023058.1:g.22650G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375631.5:c.406G= MANE Select | ENSP00000364782.4:p.Gly136= | |
| ENST00000677054.1:n.1083G= | ||
| ENST00000677512.1:n.514G= | ||
| ENST00000678869.1:n.514G= | ||
| ENST00000375631.4:c.406G= | ENSP00000364782.4:p.Gly136= | |
| ENST00000480384.1:n.435G= | ||
| ENST00000491768.5:c.406G= | ENSP00000433127.1:p.Gly136= | |
| ENST00000495807.1:n.974G= | ||
| NM_000434.3:c.406G= | NP_000425.1:p.Gly136= | |
| NM_000434.4:c.406G= MANE Select | NP_000425.1:p.Gly136= |