Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.16326507C>A , CM000668.2:g.16326507C>A | GRCh38 |
| NC_000006.11:g.16326738C>A , CM000668.1:g.16326738C>A | GRCh37 |
| NC_000006.10:g.16434717C>A | NCBI36 |
| NG_011571.1:g.439984G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001128164.2:c.1804G>T MANE Select | NP_001121636.1:p.Ala602Ser |
| ENST00000436367.6:c.1804G>T MANE Select | ENSP00000416360.1:p.Ala602Ser |
| NM_000332.3:c.1804G>T | NP_000323.2:p.Ala602Ser |
| NM_000332.4:c.1804G>T | NP_000323.2:p.Ala602Ser |
| NM_001128164.1:c.1804G>T | NP_001121636.1:p.Ala602Ser |
| NM_001357857.1:c.*1217G>T | NP_001344786.1:n.*1217G>T |
| NM_001357857.2:c.*1217G>T | NP_001344786.1:n.*1217G>T |
| ENST00000244769.8:c.1804G>T | ENSP00000244769.3:p.Ala602Ser |
| ENST00000436367.5:c.1804G>T | ENSP00000416360.1:p.Ala602Ser |