Linked Data
gnomAD v4:
5-177992635-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.177992635G>T , CM000667.2:g.177992635G>T | GRCh38 |
| NC_000005.9:g.177419636G>T , CM000667.1:g.177419636G>T | GRCh37 |
| NC_000005.8:g.177352242G>T | NCBI36 |
| NG_015889.1:g.8608C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000308304.2:c.*74C>A MANE Select | ENSP00000311290.2:n.*74C>A | |
| NM_006261.4:c.*74C>A | NP_006252.3:n.*74C>A | |
| NM_006261.5:c.*74C>A MANE Select | NP_006252.4:n.*74C>A |