Linked Data
gnomAD v4:
16-73679899-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.73679899C>A , CM000678.2:g.73679899C>A | GRCh38 |
| NC_000016.9:g.73713798C>A , CM000678.1:g.73713798C>A | GRCh37 |
| NC_000016.8:g.72271299C>A | NCBI36 |
| NG_013211.2:g.217033G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000641018.1:n.442G>T | ||
| ENST00000641206.2:c.-1547+281G>T | ENSP00000493252.1:n.-1547+281G>T | |
| ENST00000642085.1:n.163+281G>T | ||
| XR_933730.1:n.355+281G>T | ||
| XM_024450275.1:c.-494+281G>T | XP_024306043.1:n.-494+281G>T | |
| NM_001386735.1:c.-1064+281G>T | NP_001373664.1:n.-1064+281G>T |