Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.60441351G= , CM000673.2:g.60441351G= | GRCh38 |
| NC_000011.9:g.60208824G= , CM000673.1:g.60208824G= | GRCh37 |
| NC_000011.8:g.59965400G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_023945.3:c.493-6298G= MANE Select | NP_076434.2:n.493-6298G= |
| ENST00000300190.7:c.493-6298G= MANE Select | ENSP00000300190.2:n.493-6298G= |
| NM_023945.2:c.493-6298G= | NP_076434.2:n.493-6298G= |
| ENST00000300190.6:c.493-6298G= | ENSP00000300190.2:n.493-6298G= |
| ENST00000528093.1:c.136-6298G= | |
| ENST00000528905.1:c.260-6298G= | |
| ENST00000531403.5:c.*101-6298G= | ENSP00000435192.1:n.*101-6298G= |
| ENST00000533885.5:c.*103+5836G= | ENSP00000435330.1:n.*103+5836G= |