Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31859752G>C , CM000668.2:g.31859752G>C | GRCh38 |
| NC_000006.11:g.31827529G>C , CM000668.1:g.31827529G>C | GRCh37 |
| NC_000006.10:g.31935508G>C | NCBI36 |
| NG_008201.1:g.8181C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000375631.5:c.1215C>G MANE Select | ENSP00000364782.4:p.Ser405= | |
| ENST00000677054.1:n.2554C>G | ||
| ENST00000677512.1:n.1492C>G | ||
| ENST00000678869.1:n.1803C>G | ||
| ENST00000375631.4:c.1215C>G | ENSP00000364782.4:p.Ser405= | |
| ENST00000480384.1:n.1514C>G | ||
| ENST00000491768.5:c.*325C>G | ENSP00000433127.1:n.*325C>G | |
| ENST00000495807.1:n.2523C>G | ||
| NM_000434.3:c.1215C>G | NP_000425.1:p.Ser405= | |
| NM_000434.4:c.1215C>G MANE Select | NP_000425.1:p.Ser405= |