Linked Data
gnomAD v4:
8-615841-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.615841C>A , CM000670.2:g.615841C>A | GRCh38 |
| NC_000008.10:g.565841C>A , CM000670.1:g.565841C>A | GRCh37 |
| NC_000008.9:g.555841C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000522706.5:c.977-557G>T | ENSP00000428635.1:n.977-557G>T | |
| ENST00000523415.5:c.2538G>T | ||
| NM_001303100.1:c.*730G>T | NP_001290029.1:n.*730G>T | |
| XM_011534732.1:c.1442-557G>T | XP_011533034.1:n.1442-557G>T | |
| XM_011534735.1:c.*2165G>T | XP_011533037.1:n.*2165G>T | |
| XM_011534735.3:c.*2165G>T | XP_011533037.1:n.*2165G>T | |
| XM_017013124.2:c.1457-557G>T | XP_016868613.1:n.1457-557G>T | |
| NM_001303100.2:c.*730G>T | NP_001290029.1:n.*730G>T |