Linked Data
dbSNP Id:
rs746394301
ExAC:
16:72094075 C / T
gnomAD v2:
16-72094075-C-T
gnomAD v4:
16-72060176-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.72060176C>T , CM000678.2:g.72060176C>T | GRCh38 |
| NC_000016.9:g.72094075C>T , CM000678.1:g.72094075C>T | GRCh37 |
| NC_000016.8:g.70651576C>T | NCBI36 |
| NG_012651.1:g.10568C>T | |
| NG_030311.1:g.1951C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355906.10:c.507C>T (HP) MANE Select | ENSP00000348170.5:p.Ala169= | |
| ENST00000228226.12:c.132C>T (HP) | ENSP00000228226.9:p.Ala44= | |
| ENST00000355906.9:c.507C>T (HP) | ENSP00000348170.5:p.Ala169= | |
| ENST00000357763.8:c.615C>T (HP) | ENSP00000350406.5:p.Ala205= | |
| ENST00000398131.6:c.330C>T (HP) | ENSP00000381199.2:p.Ala110= | |
| ENST00000562153.5:c.285-15819G>A (TXNL4B) | ENSP00000454635.1:n.285-15819G>A | |
| ENST00000562526.5:c.266-487C>T (HP) | ENSP00000454413.1:n.266-487C>T | |
| ENST00000564499.5:c.266-56C>T (HP) | ENSP00000456503.1:n.266-56C>T | |
| ENST00000565574.5:c.330C>T (HP) | ENSP00000454966.1:p.Ala110= | |
| ENST00000566821.1:n.2146C>T (HP) | ||
| ENST00000567185.7:c.499C>T (HP) | ||
| ENST00000567612.2:c.438-56C>T (HP) | ||
| ENST00000570083.5:c.330C>T (HP) | ENSP00000457629.1:p.Ala110= | |
| ENST00000613898.1:c.132C>T (HP) | ENSP00000478279.1:p.Ala44= | |
| NM_001126102.1:c.330C>T (HP) | NP_001119574.1:p.Ala110= | |
| NM_005143.3:c.507C>T (HP) | NP_005134.1:p.Ala169= | |
| XM_005255922.3:c.330C>T (HP) | XP_005255979.2:p.Ala110= | |
| NM_001126102.2:c.330C>T (HP) | NP_001119574.1:p.Ala110= | |
| NM_001318138.1:c.330C>T (HP) | NP_001305067.1:p.Ala110= | |
| NM_005143.4:c.507C>T (HP) | NP_005134.1:p.Ala169= | |
| XM_017023377.2:c.285-15819G>A (TXNL4B) | XP_016878866.1:n.285-15819G>A | |
| NM_001318138.2:c.330C>T (HP) | NP_001305067.1:p.Ala110= | |
| NM_005143.5:c.507C>T (HP) MANE Select | NP_005134.1:p.Ala169= | |
| NM_001126102.3:c.330C>T (HP) | NP_001119574.1:p.Ala110= |