Linked Data
ClinVar Variation Id:
263413
dbSNP Id:
rs139881155
ExAC:
3:30729937 C / T
gnomAD v2:
3-30729937-C-T
gnomAD v3:
3-30688445-C-T
gnomAD v4:
3-30688445-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.30688445C>T , CM000665.2:g.30688445C>T | GRCh38 |
| NC_000003.11:g.30729937C>T , CM000665.1:g.30729937C>T | GRCh37 |
| NC_000003.10:g.30704941C>T | NCBI36 |
| NG_007490.1:g.86944C>T , LRG_779:g.86944C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000295754.10:c.1458C>T MANE Select | ENSP00000295754.5:p.Ser486= | |
| ENST00000672050.1:n.342C>T | ||
| ENST00000672866.1:n.3054C>T | ||
| ENST00000673203.1:n.336C>T | ||
| ENST00000295754.9:c.1458C>T | ENSP00000295754.5:p.Ser486= | |
| ENST00000359013.4:c.1533C>T | ENSP00000351905.4:p.Ser511= | |
| NM_001024847.2:c.1533C>T , LRG_779t1:c.1533C>T | NP_001020018.1:p.Ser511= | |
| NM_003242.5:c.1458C>T | NP_003233.4:p.Ser486= | |
| XM_011534043.1:c.1485C>T | XP_011532345.1:p.Ser495= | |
| XM_011534044.1:c.1410C>T | XP_011532346.1:p.Ser470= | |
| XM_011534045.1:c.1353C>T | XP_011532347.1:p.Ser451= | |
| XM_011534043.2:c.1485C>T | XP_011532345.1:p.Ser495= | |
| XM_011534045.3:c.1353C>T | XP_011532347.1:p.Ser451= | |
| XM_017007106.1:c.1353C>T | XP_016862595.1:p.Ser451= | |
| NM_003242.6:c.1458C>T MANE Select | NP_003233.4:p.Ser486= |