Linked Data
gnomAD v4:
5-128300827-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.128300827C>A , CM000667.2:g.128300827C>A | GRCh38 |
| NC_000005.9:g.127636519C>A , CM000667.1:g.127636519C>A | GRCh37 |
| NC_000005.8:g.127664418C>A | NCBI36 |
| NG_008750.1:g.242217G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000703783.1:n.2940G>T | ||
| ENST00000703785.1:n.2859G>T | ||
| ENST00000262464.9:c.6156G>T MANE Select | ENSP00000262464.4:p.Glu2052Asp | |
| ENST00000262464.8:c.6156G>T | ENSP00000262464.4:p.Glu2052Asp | |
| ENST00000508053.5:c.6156G>T | ENSP00000424571.1:p.Glu2052Asp | |
| ENST00000619499.4:c.6153G>T | ENSP00000482132.1:p.Glu2051Asp | |
| NM_001999.3:c.6156G>T | NP_001990.2:p.Glu2052Asp | |
| XM_017009228.2:c.6003G>T | XP_016864717.1:p.Glu2001Asp | |
| NM_001999.4:c.6156G>T MANE Select | NP_001990.2:p.Glu2052Asp |