Linked Data
ClinVar Variation Id:
346474
dbSNP Id:
rs745530308
ExAC:
3:64132849 G / A
gnomAD v2:
3-64132849-G-A
gnomAD v3:
3-64147173-G-A
gnomAD v4:
3-64147173-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.64147173G>A , CM000665.2:g.64147173G>A | GRCh38 |
| NC_000003.11:g.64132849G>A , CM000665.1:g.64132849G>A | GRCh37 |
| NC_000003.10:g.64107889G>A | NCBI36 |
| NG_031930.1:g.83283C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000295902.11:c.1485C>T | ENSP00000295902.7:p.Pro495= | |
| ENST00000564377.6:c.1317C>T | ENSP00000455004.2:p.Pro439= | |
| ENST00000638394.2:c.1317C>T MANE Select | ENSP00000492363.1:p.Pro439= | |
| ENST00000640095.1:n.2385C>T | ||
| ENST00000640303.1:n.1956C>T | ||
| ENST00000295902.10:c.1317C>T | ENSP00000295902.6:p.Pro439= | |
| ENST00000564377.5:c.1485C>T | ENSP00000455004.1:p.Pro495= | |
| NM_198859.3:c.1317C>T | NP_942559.1:p.Pro439= | |
| XM_011533432.1:c.1593C>T | XP_011531734.1:p.Pro531= | |
| XM_011533433.1:c.1593C>T | XP_011531735.1:p.Pro531= | |
| XM_011533434.1:c.1485C>T | XP_011531736.1:p.Pro495= | |
| XM_011533435.1:c.1485C>T | XP_011531737.1:p.Pro495= | |
| XM_011533436.1:c.1317C>T | XP_011531738.1:p.Pro439= | |
| XM_011533437.1:c.1317C>T | XP_011531739.1:p.Pro439= | |
| XM_011533438.1:c.966C>T | XP_011531740.1:p.Pro322= | |
| XM_011533439.1:c.1317C>T | XP_011531741.1:p.Pro439= | |
| XM_011533440.1:c.1593C>T | XP_011531742.1:p.Pro531= | |
| XM_011533432.2:c.1593C>T | XP_011531734.1:p.Pro531= | |
| XM_011533433.2:c.1593C>T | XP_011531735.1:p.Pro531= | |
| XM_011533434.2:c.1485C>T | XP_011531736.1:p.Pro495= | |
| XM_011533435.2:c.1485C>T | XP_011531737.1:p.Pro495= | |
| XM_011533436.3:c.1317C>T | XP_011531738.1:p.Pro439= | |
| XM_011533437.2:c.1317C>T | XP_011531739.1:p.Pro439= | |
| XM_011533438.2:c.966C>T | XP_011531740.1:p.Pro322= | |
| XM_011533440.2:c.1593C>T | XP_011531742.1:p.Pro531= | |
| XM_017005798.1:c.1317C>T | XP_016861287.1:p.Pro439= | |
| XM_017005799.1:c.945C>T | XP_016861288.1:p.Pro315= | |
| NM_198859.4:c.1317C>T MANE Select | NP_942559.1:p.Pro439= | |
| NM_001370528.1:c.1317C>T | NP_001357457.1:p.Pro439= |