Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.116832939T>C , CM000673.2:g.116832939T>C | GRCh38 |
| NC_000011.9:g.116703655T>C , CM000673.1:g.116703655T>C | GRCh37 |
| NC_000011.8:g.116208865T>C | NCBI36 |
| NG_008949.1:g.8032T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000227667.8:c.*55T>C MANE Select | ENSP00000227667.2:n.*55T>C | |
| ENST00000227667.7:c.*55T>C | ENSP00000227667.2:n.*55T>C | |
| ENST00000375345.3:c.*55T>C | ENSP00000364494.1:n.*55T>C | |
| ENST00000630701.1:c.409T>C | ENSP00000486182.1:n.409T>C | |
| NM_000040.1:c.*55T>C | NP_000031.1:n.*55T>C | |
| NM_000040.2:c.*55T>C | NP_000031.1:n.*55T>C | |
| NM_000040.3:c.*55T>C MANE Select | NP_000031.1:n.*55T>C |