Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.104053064C= , CM000672.2:g.104053064C= | GRCh38 |
| NC_000010.10:g.105812822C= , CM000672.1:g.105812822C= | GRCh37 |
| NC_000010.9:g.105802812C= | NCBI36 |
| NG_007069.1:g.37817G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000494.4:c.1906G= MANE Select | NP_000485.3:p.Gly636= |
| ENST00000648076.2:c.1906G= MANE Select | ENSP00000497653.1:p.Gly636= |
| NM_000494.3:c.1906G= | NP_000485.3:p.Gly636= |
| ENST00000353479.9:c.1906G= | ENSP00000340937.5:p.Gly636= |
| ENST00000369733.7:c.1906G= | ENSP00000358748.3:p.Gly636= |
| ENST00000369733.8:c.1906G= | ENSP00000358748.3:p.Gly636= |