Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.48898688A>C , CM000665.2:g.48898688A>C | GRCh38 |
| NC_000003.11:g.48936121A>C , CM000665.1:g.48936121A>C | GRCh37 |
| NC_000003.10:g.48911125A>C | NCBI36 |
| NG_008171.1:g.5209T>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000387.6:c.105+2T>G MANE Select | NP_000378.1:n.105+2T>G |
| ENST00000319017.5:c.105+2T>G MANE Select | ENSP00000326305.4:n.105+2T>G |
| NM_000387.5:c.105+2T>G | NP_000378.1:n.105+2T>G |
| ENST00000319017.4:c.105+2T>G | ENSP00000326305.4:n.105+2T>G |
| ENST00000430379.5:c.105+2T>G | ENSP00000388986.1:n.105+2T>G |
| ENST00000440964.1:c.105+2T>G | ENSP00000388563.1:n.105+2T>G |
| XM_006713327.1:c.105+2T>G | XP_006713390.1:n.105+2T>G |