Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.20579812C>T , CM000686.2:g.20579812C>T | GRCh38 |
| NC_000024.9:g.22741698C>T , CM000686.1:g.22741698C>T | GRCh37 |
| NC_000024.8:g.21151086C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000361365.7:c.100+121C>T MANE Select | ENSP00000354722.2:n.100+121C>T | |
| ENST00000361365.6:c.100+121C>T | ENSP00000354722.2:n.100+121C>T | |
| ENST00000382772.3:c.100+121C>T | ENSP00000372222.3:n.100+121C>T | |
| ENST00000465253.1:n.194+121C>T | ||
| NM_001278612.1:c.100+121C>T | NP_001265541.1:n.100+121C>T | |
| NM_004681.3:c.100+121C>T | NP_004672.2:n.100+121C>T | |
| NM_004681.4:c.100+121C>T MANE Select | NP_004672.2:n.100+121C>T | |
| NM_001278612.2:c.100+121C>T | NP_001265541.1:n.100+121C>T |