Linked Data
ClinVar Variation Id:
3000772
ClinVar RCV Id:
RCV003859931
dbSNP Id:
rs1699392307
gnomAD v4:
3-30674131-A-G
MyVariant Identifiers:
chr3:g.30715623A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.30674131A>G , CM000665.2:g.30674131A>G | GRCh38 |
| NC_000003.11:g.30715623A>G , CM000665.1:g.30715623A>G | GRCh37 |
| NC_000003.10:g.30690627A>G | NCBI36 |
| NG_007490.1:g.72630A>G , LRG_779:g.72630A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000295754.10:c.1281A>G MANE Select | ENSP00000295754.5:p.Pro427= | |
| ENST00000672866.1:n.2877A>G | ||
| ENST00000673203.1:n.159A>G | ||
| ENST00000295754.9:c.1281A>G | ENSP00000295754.5:p.Pro427= | |
| ENST00000359013.4:c.1356A>G | ENSP00000351905.4:p.Pro452= | |
| NM_001024847.2:c.1356A>G , LRG_779t1:c.1356A>G | NP_001020018.1:p.Pro452= | |
| NM_003242.5:c.1281A>G | NP_003233.4:p.Pro427= | |
| XM_011534043.1:c.1308A>G | XP_011532345.1:p.Pro436= | |
| XM_011534044.1:c.1233A>G | XP_011532346.1:p.Pro411= | |
| XM_011534045.1:c.1176A>G | XP_011532347.1:p.Pro392= | |
| XM_011534043.2:c.1308A>G | XP_011532345.1:p.Pro436= | |
| XM_011534045.3:c.1176A>G | XP_011532347.1:p.Pro392= | |
| XM_017007106.1:c.1176A>G | XP_016862595.1:p.Pro392= | |
| NM_003242.6:c.1281A>G MANE Select | NP_003233.4:p.Pro427= |