Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.5951841C>G , CM000674.2:g.5951841C>G | GRCh38 |
| NC_000012.11:g.6061007C>G , CM000674.1:g.6061007C>G | GRCh37 |
| NC_000012.10:g.5931268C>G | NCBI36 |
| NG_009072.1:g.177830G>C | |
| NG_009072.2:g.177830G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261405.10:c.8155+3G>C MANE Select | ENSP00000261405.5:n.8155+3G>C | |
| ENST00000261405.9:c.8155+3G>C | ENSP00000261405.5:n.8155+3G>C | |
| NM_000552.3:c.8155+3G>C | NP_000543.2:n.8155+3G>C | |
| NM_000552.4:c.8155+3G>C | NP_000543.2:n.8155+3G>C | |
| NM_000552.5:c.8155+3G>C MANE Select | NP_000543.3:n.8155+3G>C |