Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.640862G>C , CM000685.2:g.640862G>C | GRCh38 |
| NC_000023.10:g.601597G>C , CM000685.1:g.601597G>C | GRCh37 |
| NC_000023.9:g.521597G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| ENST00000686671.1:c.528G>C MANE Select | ENSP00000508521.1:p.Glu176Asp |
| ENST00000334060.8:c.528G>C | ENSP00000335505.3:p.Glu176Asp |
| ENST00000381575.6:c.528G>C | ENSP00000370987.1:p.Glu176Asp |
| ENST00000381578.6:c.528G>C | ENSP00000370990.1:p.Glu176Asp |
| ENST00000554971.6:c.528G>C | ENSP00000452016.1:p.Glu176Asp |