Linked Data
dbSNP Id:
rs759653973
ExAC:
11:67353694 G / A
gnomAD v2:
11-67353694-G-A
gnomAD v4:
11-67586223-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67586223G>A , CM000673.2:g.67586223G>A | GRCh38 |
| NC_000011.9:g.67353694G>A , CM000673.1:g.67353694G>A | GRCh37 |
| NC_000011.8:g.67110270G>A | NCBI36 |
| NG_012075.1:g.7629G>A , LRG_723:g.7629G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000398603.6:c.337-166G>A | ENSP00000381604.1:n.337-166G>A | |
| ENST00000398606.10:c.444+12G>A MANE Select | ENSP00000381607.3:n.444+12G>A | |
| ENST00000646888.1:c.*160+12G>A | ENSP00000494477.1:n.*160+12G>A | |
| ENST00000398603.5:c.337-166G>A | ENSP00000381604.1:n.337-166G>A | |
| ENST00000398606.7:c.444+12G>A | ENSP00000381607.3:n.444+12G>A | |
| ENST00000467591.1:n.555+12G>A | ||
| ENST00000494593.1:n.1251G>A | ||
| ENST00000495996.1:c.120G>A | ENSP00000484686.1:p.Trp40Ter | |
| ENST00000498765.5:c.507+12G>A | ||
| NM_000852.3:c.444+12G>A , LRG_723t1:c.444+12G>A | NP_000843.1:n.444+12G>A | |
| NM_000852.4:c.444+12G>A MANE Select | NP_000843.1:n.444+12G>A |