Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.2866813C= , CM000686.2:g.2866813C= | GRCh38 |
| NC_000024.9:g.2734854C= , CM000686.1:g.2734854C= | GRCh37 |
| NC_000024.8:g.2794854C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000250784.13:c.711C= MANE Select | ENSP00000250784.7:p.Ser237= | |
| ENST00000250784.12:c.711C= | ENSP00000250784.7:p.Ser237= | |
| ENST00000430575.1:c.738C= | ENSP00000415317.1:p.Ser246= | |
| ENST00000477725.1:n.855C= | ||
| ENST00000515575.1:n.42+12042C= | ||
| NM_001008.3:c.711C= | NP_000999.1:p.Ser237= | |
| NM_001008.4:c.711C= MANE Select | NP_000999.1:p.Ser237= |