Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.96204878A= , CM000676.2:g.96204878A= | GRCh38 |
| NC_000014.8:g.96671215A= , CM000676.1:g.96671215A= | GRCh37 |
| NC_000014.7:g.95740968A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000554311.2:c.-121A= MANE Select | ENSP00000450482.1:n.-121A= | |
| ENST00000539359.1:c.-363A= | ENSP00000438376.1:n.-363A= | |
| ENST00000542454.2:c.-2889A= | ENSP00000439459.2:n.-2889A= | |
| ENST00000553811.1:c.-116A= | ENSP00000450984.1:n.-116A= | |
| ENST00000554311.1:c.-121A= | ENSP00000450482.1:n.-121A= | |
| NM_000623.3:c.-116A= | NP_000614.1:n.-116A= | |
| NM_000623.4:c.-116A= | NP_000614.1:n.-116A= | |
| NM_001379692.1:c.-121A= MANE Select | NP_001366621.1:n.-121A= |