Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.55043675A= , CM000663.2:g.55043675A= | GRCh38 |
| NC_000001.10:g.55509348A= , CM000663.1:g.55509348A= | GRCh37 |
| NC_000001.9:g.55281936A= | NCBI36 |
| NG_009061.1:g.9129A= , LRG_275:g.9129A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000673913.2:c.208-168A= | ENSP00000501161.2:n.208-168A= | |
| ENST00000710286.1:c.565-168A= | ENSP00000518176.1:n.565-168A= | |
| ENST00000673726.1:c.208-168A= | ENSP00000501004.1:n.208-168A= | |
| ENST00000673903.1:c.-168-168A= | ENSP00000501257.1:n.-168-168A= | |
| ENST00000302118.5:c.208-168A= MANE Select | ENSP00000303208.5:n.208-168A= | |
| NM_174936.3:c.208-168A= , LRG_275t1:c.208-168A= | NP_777596.2:n.208-168A= | |
| NR_110451.1:n.182+3272A= | ||
| NM_174936.4:c.208-168A= MANE Select | NP_777596.2:n.208-168A= | |
| NR_110451.2:n.182+3272A= |