Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.119672413G= , CM000672.2:g.119672413G= | GRCh38 |
| NC_000010.10:g.121431925G= , CM000672.1:g.121431925G= | GRCh37 |
| NC_000010.9:g.121421915G= | NCBI36 |
| NG_016125.1:g.26044G= , LRG_742:g.26044G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369085.8:c.666G= MANE Select | ENSP00000358081.4:p.Gln222= | |
| ENST00000369085.7:c.666G= | ENSP00000358081.3:p.Gln222= | |
| ENST00000450186.1:c.492G= | ENSP00000410036.1:p.Gln164= | |
| NM_004281.3:c.666G= , LRG_742t1:c.666G= | NP_004272.2:p.Gln222= | |
| XM_005270287.1:c.666G= | XP_005270344.1:p.Gln222= | |
| XM_005270287.2:c.666G= | XP_005270344.1:p.Gln222= | |
| NM_004281.4:c.666G= MANE Select | NP_004272.2:p.Gln222= |