Linked Data
dbSNP Id:
rs1413034880
gnomAD v2:
11-6638515-C-T
gnomAD v3:
11-6617284-C-T
gnomAD v4:
11-6617284-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.6617284C>T , CM000673.2:g.6617284C>T | GRCh38 |
| NC_000011.9:g.6638515C>T , CM000673.1:g.6638515C>T | GRCh37 |
| NC_000011.8:g.6595091C>T | NCBI36 |
| NG_008653.1:g.7178G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682424.1:c.394+17G>A | ENSP00000507321.1:n.394+17G>A | |
| ENST00000299427.12:c.508+17G>A MANE Select | ENSP00000299427.6:n.508+17G>A | |
| ENST00000428886.7:n.613G>A | ||
| ENST00000436873.7:c.312+17G>A | ||
| ENST00000524788.2:n.1537G>A | ||
| ENST00000524903.2:n.1653G>A | ||
| ENST00000528571.6:c.*265G>A | ENSP00000434647.1:n.*265G>A | |
| ENST00000528807.2:n.164+17G>A | ||
| ENST00000530040.2:n.479+75G>A | ||
| ENST00000533371.6:c.-222+17G>A | ENSP00000437066.1:n.-222+17G>A | |
| ENST00000534644.6:n.456+70G>A | ||
| ENST00000642892.1:c.-222+70G>A | ENSP00000494165.1:n.-222+70G>A | |
| ENST00000643439.1:c.*248+17G>A | ENSP00000495849.1:n.*248+17G>A | |
| ENST00000643479.1:n.537+17G>A | ||
| ENST00000643516.1:c.395+17G>A | ||
| ENST00000644151.1:n.1817G>A | ||
| ENST00000644218.1:c.508+17G>A | ENSP00000493574.1:n.508+17G>A | |
| ENST00000644683.1:c.450+75G>A | ENSP00000494085.1:n.450+75G>A | |
| ENST00000644810.1:c.230-131G>A | ENSP00000495895.1:n.230-131G>A | |
| ENST00000644831.1:n.554G>A | ||
| ENST00000644933.1:c.-222+17G>A | ENSP00000496133.1:n.-222+17G>A | |
| ENST00000645020.1:n.1553G>A | ||
| ENST00000645285.1:c.-222+17G>A | ENSP00000495058.1:n.-222+17G>A | |
| ENST00000645331.1:n.744G>A | ||
| ENST00000645620.1:c.-222+75G>A | ENSP00000493657.1:n.-222+75G>A | |
| ENST00000646777.1:n.554G>A | ||
| ENST00000647016.1:n.858G>A | ||
| ENST00000647152.1:c.-222+17G>A | ENSP00000495893.1:n.-222+17G>A | |
| ENST00000647209.1:c.*377+17G>A | ENSP00000495558.1:n.*377+17G>A | |
| ENST00000647346.1:n.1528+17G>A | ||
| ENST00000299427.10:c.508+17G>A | ENSP00000299427.6:n.508+17G>A | |
| ENST00000428886.6:n.547G>A | ||
| ENST00000436873.6:c.450+75G>A | ENSP00000398136.2:n.450+75G>A | |
| ENST00000524788.1:n.78G>A | ||
| ENST00000528571.5:c.*248+17G>A | ENSP00000434647.1:n.*248+17G>A | |
| ENST00000533371.5:c.-222+17G>A | ENSP00000437066.1:n.-222+17G>A | |
| ENST00000534644.5:n.493+17G>A | ||
| ENST00000611494.4:c.508+17G>A | ENSP00000484546.1:n.508+17G>A | |
| NM_000391.3:c.508+17G>A | NP_000382.3:n.508+17G>A | |
| NM_000391.4:c.508+17G>A MANE Select | NP_000382.3:n.508+17G>A |