Linked Data
dbSNP Id:
rs897876667
gnomAD v2:
16-73713692-C-T
gnomAD v3:
16-73679793-C-T
gnomAD v4:
16-73679793-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.73679793C>T , CM000678.2:g.73679793C>T | GRCh38 |
| NC_000016.9:g.73713692C>T , CM000678.1:g.73713692C>T | GRCh37 |
| NC_000016.8:g.72271193C>T | NCBI36 |
| NG_013211.2:g.217139G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000641018.1:n.548G>A | ||
| ENST00000641206.2:c.-1547+387G>A | ENSP00000493252.1:n.-1547+387G>A | |
| ENST00000642085.1:n.163+387G>A | ||
| XR_933730.1:n.355+387G>A | ||
| XM_024450275.1:c.-494+387G>A | XP_024306043.1:n.-494+387G>A | |
| NM_001386735.1:c.-1064+387G>A | NP_001373664.1:n.-1064+387G>A |