Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154984682C>G , CM000685.2:g.154984682C>G | GRCh38 |
| NC_000023.10:g.154212957C>G , CM000685.1:g.154212957C>G | GRCh37 |
| NC_000023.9:g.153866151C>G | NCBI36 |
| NG_011403.1:g.43042G>C | |
| NG_011403.2:g.43042G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000132.4:c.787+5G>C MANE Select | NP_000123.1:n.787+5G>C |
| ENST00000360256.9:c.787+5G>C MANE Select | ENSP00000353393.4:n.787+5G>C |
| NM_000132.3:c.787+5G>C | NP_000123.1:n.787+5G>C |
| ENST00000360256.8:c.787+5G>C | ENSP00000353393.4:n.787+5G>C |
| ENST00000647125.1:c.*573+5G>C | ENSP00000496062.1:n.*573+5G>C |
| XM_011531126.1:c.682+5G>C | XP_011529428.1:n.682+5G>C |