Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.14716767G= , CM000667.2:g.14716767G= | GRCh38 |
| NC_000005.9:g.14716876G= , CM000667.1:g.14716876G= | GRCh37 |
| NC_000005.8:g.14769876G= | NCBI36 |
| NG_008273.1:g.160012C= | |
| NG_008273.2:g.160019C= | |
| NG_051625.1:g.60974G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000284268.8:c.1080C= MANE Select | ENSP00000284268.6:p.Asp360= | |
| ENST00000284268.6:c.1080C= | ENSP00000284268.6:p.Asp360= | |
| ENST00000502585.1:n.322C= | ||
| NM_054027.4:c.1080C= | NP_473368.1:p.Asp360= | |
| NM_054027.5:c.1080C= | NP_473368.1:p.Asp360= | |
| XM_017009644.2:c.996C= | XP_016865133.1:p.Asp332= | |
| NM_054027.6:c.1080C= MANE Select | NP_473368.1:p.Asp360= |