Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.159322125A>C , CM000667.2:g.159322125A>C | GRCh38 |
| NC_000005.9:g.158749133A>C , CM000667.1:g.158749133A>C | GRCh37 |
| NC_000005.8:g.158681711A>C | NCBI36 |
| NG_009618.1:g.13349T>G , LRG_71:g.13349T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696750.1:c.-148-1605T>G | ENSP00000512849.1:n.-148-1605T>G | |
| ENST00000696751.1:c.364+929T>G | ENSP00000512850.1:n.364+929T>G | |
| ENST00000231228.3:c.482+269T>G MANE Select | ENSP00000231228.2:n.482+269T>G | |
| ENST00000231228.2:c.482+269T>G | ENSP00000231228.2:n.482+269T>G | |
| NM_002187.2:c.482+269T>G , LRG_71t1:c.482+269T>G | NP_002178.2:n.482+269T>G | |
| XR_001742945.1:n.147+1529A>C | ||
| NM_002187.3:c.482+269T>G MANE Select | NP_002178.2:n.482+269T>G |