Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31862088C>G , CM000668.2:g.31862088C>G | GRCh38 |
| NC_000006.11:g.31829865C>G , CM000668.1:g.31829865C>G | GRCh37 |
| NC_000006.10:g.31937844C>G | NCBI36 |
| NG_008201.1:g.5845G>C | |
| NG_023058.1:g.21959G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000434.4:c.263G>C MANE Select | NP_000425.1:p.Gly88Ala |
| ENST00000375631.5:c.263G>C MANE Select | ENSP00000364782.4:p.Gly88Ala |
| NM_000434.3:c.263G>C | NP_000425.1:p.Gly88Ala |
| ENST00000375631.4:c.263G>C | ENSP00000364782.4:p.Gly88Ala |
| ENST00000480384.1:n.292G>C | |
| ENST00000491768.5:c.263G>C | ENSP00000433127.1:p.Gly88Ala |
| ENST00000495807.1:n.283G>C | |
| ENST00000677054.1:n.392G>C | |
| ENST00000677512.1:n.371G>C | |
| ENST00000678869.1:n.371G>C |