Linked Data
ClinVar Variation Id:
284419
dbSNP Id:
rs202215735
ExAC:
16:75590017 C / T
gnomAD v2:
16-75590017-C-T
gnomAD v3:
16-75556119-C-T
gnomAD v4:
16-75556119-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.75556119C>T , CM000678.2:g.75556119C>T | GRCh38 |
| NC_000016.9:g.75590017C>T , CM000678.1:g.75590017C>T | GRCh37 |
| NC_000016.8:g.74147518C>T | NCBI36 |
| NG_033109.1:g.5168G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000685935.1:c.91G>A | ENSP00000510128.1:p.Ala31Thr | |
| ENST00000686547.1:c.91G>A | ENSP00000508790.1:p.Ala31Thr | |
| ENST00000688270.1:c.91G>A | ENSP00000509823.1:p.Ala31Thr | |
| ENST00000688618.1:c.91G>A | ENSP00000509271.1:p.Ala31Thr | |
| ENST00000689040.1:c.91G>A | ENSP00000508573.1:p.Ala31Thr | |
| ENST00000692097.1:c.91G>A | ENSP00000509668.1:p.Ala31Thr | |
| ENST00000692215.1:n.134G>A | ||
| ENST00000693457.1:c.91G>A | ENSP00000508414.1:p.Ala31Thr | |
| ENST00000693682.1:c.91G>A | ENSP00000508670.1:p.Ala31Thr | |
| ENST00000258173.11:c.91G>A MANE Select | ENSP00000258173.5:p.Ala31Thr | |
| ENST00000258173.10:c.91G>A | ENSP00000258173.5:p.Ala31Thr | |
| ENST00000561809.1:n.144G>A | ||
| ENST00000562410.5:c.91G>A | ENSP00000454582.1:p.Ala31Thr | |
| ENST00000564576.1:n.127G>A | ||
| ENST00000565067.5:c.91G>A | ENSP00000457254.1:p.Ala31Thr | |
| ENST00000568377.5:c.81G>A | ENSP00000476267.1:p.Pro27= | |
| ENST00000570006.5:c.91G>A | ENSP00000455520.1:p.Ala31Thr | |
| NM_001077416.2:c.153G>A | NP_001070884.2:p.Pro51= | |
| NM_001077418.2:c.91G>A | NP_001070886.1:p.Ala31Thr | |
| NR_074083.1:n.168G>A | ||
| NM_001077418.3:c.91G>A MANE Select | NP_001070886.1:p.Ala31Thr | |
| NR_074083.2:n.134G>A |