Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.10568466C= , CM000681.2:g.10568466C= | GRCh38 |
| NC_000019.9:g.10679142C= , CM000681.1:g.10679142C= | GRCh37 |
| NC_000019.8:g.10540142C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000393599.3:c.141+47G= MANE Select | ENSP00000377224.1:n.141+47G= | |
| ENST00000335766.2:c.141+47G= | ENSP00000337056.1:n.141+47G= | |
| ENST00000393599.2:c.141+47G= | ENSP00000377224.1:n.141+47G= | |
| NM_001800.3:c.141+47G= | NP_001791.1:n.141+47G= | |
| NM_079421.2:c.141+47G= | NP_524145.1:n.141+47G= | |
| NM_001800.4:c.141+47G= MANE Select | NP_001791.1:n.141+47G= | |
| NM_079421.3:c.141+47G= | NP_524145.1:n.141+47G= |