Linked Data
gnomAD v4:
5-177992687-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.177992687C>A , CM000667.2:g.177992687C>A | GRCh38 |
| NC_000005.9:g.177419688C>A , CM000667.1:g.177419688C>A | GRCh37 |
| NC_000005.8:g.177352294C>A | NCBI36 |
| NG_015889.1:g.8556G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000308304.2:c.*22G>T MANE Select | ENSP00000311290.2:n.*22G>T | |
| NM_006261.4:c.*22G>T | NP_006252.3:n.*22G>T | |
| NM_006261.5:c.*22G>T MANE Select | NP_006252.4:n.*22G>T |