Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.4234910C= , CM000682.2:g.4234910C= | GRCh38 |
| NC_000020.10:g.4215557C= , CM000682.1:g.4215557C= | GRCh37 |
| NC_000020.9:g.4163557C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000678.4:c.1112-12780G= MANE Select | NP_000669.1:n.1112-12780G= |
| ENST00000379453.6:c.1112-12780G= MANE Select | ENSP00000368766.4:n.1112-12780G= |
| NM_000678.3:c.1112-12780G= | NP_000669.1:n.1112-12780G= |
| ENST00000379453.5:c.1112-12780G= | ENSP00000368766.4:n.1112-12780G= |