Linked Data
ClinVar Variation Id:
1614863
ClinVar RCV Id:
RCV002078925
dbSNP Id:
rs2125438921
MyVariant Identifiers:
chr3:g.30715638C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.30674146C>T , CM000665.2:g.30674146C>T | GRCh38 |
| NC_000003.11:g.30715638C>T , CM000665.1:g.30715638C>T | GRCh37 |
| NC_000003.10:g.30690642C>T | NCBI36 |
| NG_007490.1:g.72645C>T , LRG_779:g.72645C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000295754.10:c.1296C>T MANE Select | ENSP00000295754.5:p.Ser432= | |
| ENST00000672866.1:n.2892C>T | ||
| ENST00000673203.1:n.174C>T | ||
| ENST00000295754.9:c.1296C>T | ENSP00000295754.5:p.Ser432= | |
| ENST00000359013.4:c.1371C>T | ENSP00000351905.4:p.Ser457= | |
| NM_001024847.2:c.1371C>T , LRG_779t1:c.1371C>T | NP_001020018.1:p.Ser457= | |
| NM_003242.5:c.1296C>T | NP_003233.4:p.Ser432= | |
| XM_011534043.1:c.1323C>T | XP_011532345.1:p.Ser441= | |
| XM_011534044.1:c.1248C>T | XP_011532346.1:p.Ser416= | |
| XM_011534045.1:c.1191C>T | XP_011532347.1:p.Ser397= | |
| XM_011534043.2:c.1323C>T | XP_011532345.1:p.Ser441= | |
| XM_011534045.3:c.1191C>T | XP_011532347.1:p.Ser397= | |
| XM_017007106.1:c.1191C>T | XP_016862595.1:p.Ser397= | |
| NM_003242.6:c.1296C>T MANE Select | NP_003233.4:p.Ser432= |