Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.100045634T>C , CM000672.2:g.100045634T>C | GRCh38 |
| NC_000010.10:g.101805391T>C , CM000672.1:g.101805391T>C | GRCh37 |
| NC_000010.9:g.101795381T>C | NCBI36 |
| NG_012060.1:g.41252A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000370418.8:c.1231-3061A>G MANE Select | ENSP00000359446.3:n.1231-3061A>G | |
| ENST00000370418.7:c.1231-3061A>G | ENSP00000359446.3:n.1231-3061A>G | |
| NM_001308.2:c.1231-3061A>G | NP_001299.1:n.1231-3061A>G | |
| XM_011539299.1:c.1273-3061A>G | XP_011537601.1:n.1273-3061A>G | |
| NM_001308.3:c.1231-3061A>G MANE Select | NP_001299.1:n.1231-3061A>G |