Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.117818433A>C , CM000670.2:g.117818433A>C | GRCh38 |
| NC_000008.10:g.118830672A>C , CM000670.1:g.118830672A>C | GRCh37 |
| NC_000008.9:g.118899853A>C | NCBI36 |
| NG_007455.2:g.298387T>G , LRG_493:g.298387T>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000127.3:c.1632+2T>G MANE Select | NP_000118.2:n.1632+2T>G |
| ENST00000378204.7:c.1632+2T>G MANE Select | ENSP00000367446.3:n.1632+2T>G |
| NM_000127.2:c.1632+2T>G , LRG_493t1:c.1632+2T>G | NP_000118.2:n.1632+2T>G |
| ENST00000378204.6:c.1632+2T>G | ENSP00000367446.2:n.1632+2T>G |
| ENST00000437196.1:c.*523+2T>G | ENSP00000407299.1:n.*523+2T>G |
| ENST00000684189.1:n.1099+2T>G |