Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.80778838T>C , CM000667.2:g.80778838T>C | GRCh38 |
| NC_000005.9:g.80074657T>C , CM000667.1:g.80074657T>C | GRCh37 |
| NC_000005.8:g.80110413T>C | NCBI36 |
| NG_016607.1:g.129364T>C | |
| NG_016607.2:g.129364T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002439.5:c.2435+2T>C MANE Select | NP_002430.3:n.2435+2T>C |
| ENST00000265081.7:c.2435+2T>C MANE Select | ENSP00000265081.6:n.2435+2T>C |
| NM_002439.4:c.2435+2T>C | NP_002430.3:n.2435+2T>C |
| ENST00000265081.6:c.2435+2T>C | ENSP00000265081.6:n.2435+2T>C |
| ENST00000658259.1:c.2267+2T>C | ENSP00000499617.1:n.2267+2T>C |
| ENST00000667069.1:c.2240+2T>C | ENSP00000499502.1:n.2240+2T>C |
| ENST00000670357.1:c.2435+2T>C | ENSP00000499791.1:n.2435+2T>C |