Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.102208052C= , CM000670.2:g.102208052C= | GRCh38 |
| NC_000008.10:g.103220280C= , CM000670.1:g.103220280C= | GRCh37 |
| NC_000008.9:g.103289456C= | NCBI36 |
| NG_016617.1:g.36067G= , LRG_788:g.36067G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000251810.8:c.*81G= MANE Select | ENSP00000251810.3:n.*81G= | |
| ENST00000251810.7:c.*81G= | ENSP00000251810.3:n.*81G= | |
| ENST00000395910.6:n.524G= | ||
| ENST00000522368.5:c.1306G= | ||
| ENST00000621845.1:c.*81G= | ENSP00000484318.1:n.*81G= | |
| NM_001172477.1:c.*81G= , LRG_788t1:c.*81G= | NP_001165948.1:n.*81G= | |
| NM_001172478.1:c.*81G= | NP_001165949.1:n.*81G= | |
| NM_015713.4:c.*81G= , LRG_788t2:c.*81G= | NP_056528.2:n.*81G= | |
| NM_001172478.2:c.*81G= | NP_001165949.1:n.*81G= | |
| NM_015713.5:c.*81G= MANE Select | NP_056528.2:n.*81G= |