Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.96204926G= , CM000676.2:g.96204926G= | GRCh38 |
| NC_000014.8:g.96671263G= , CM000676.1:g.96671263G= | GRCh37 |
| NC_000014.7:g.95741016G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000554311.2:c.-73G= MANE Select | ENSP00000450482.1:n.-73G= | |
| ENST00000539359.1:c.-315G= | ENSP00000438376.1:n.-315G= | |
| ENST00000542454.2:c.-2841G= | ENSP00000439459.2:n.-2841G= | |
| ENST00000553811.1:c.-68G= | ENSP00000450984.1:n.-68G= | |
| ENST00000554311.1:c.-73G= | ENSP00000450482.1:n.-73G= | |
| NM_000623.3:c.-68G= | NP_000614.1:n.-68G= | |
| NM_000623.4:c.-68G= | NP_000614.1:n.-68G= | |
| NM_001379692.1:c.-73G= MANE Select | NP_001366621.1:n.-73G= |