Linked Data
ClinVar Variation Id:
1603820
ClinVar RCV Id:
RCV003033298
dbSNP Id:
rs2042516875
gnomAD v3:
3-49104662-G-C
gnomAD v4:
3-49104662-G-C
MyVariant Identifiers:
chr3:g.49142095G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.49104662G>C , CM000665.2:g.49104662G>C | GRCh38 |
| NC_000003.11:g.49142095G>C , CM000665.1:g.49142095G>C | GRCh37 |
| NC_000003.10:g.49117099G>C | NCBI36 |
| NG_042312.1:g.5468C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000306125.12:c.72C>G MANE Select | ENSP00000307567.6:p.Leu24= | |
| ENST00000306125.11:c.72C>G | ENSP00000307567.6:p.Leu24= | |
| ENST00000414533.5:c.72C>G | ENSP00000390015.1:p.Leu24= | |
| ENST00000417025.2:n.98C>G | ||
| ENST00000418549.3:c.72C>G | ENSP00000415247.1:p.Leu24= | |
| ENST00000430182.5:c.72C>G | ENSP00000389823.1:p.Leu24= | |
| ENST00000452739.5:c.72C>G | ENSP00000392850.2:p.Leu24= | |
| ENST00000470619.6:n.91C>G | ||
| ENST00000479495.5:n.98-191C>G | ||
| ENST00000482261.7:n.148C>G | ||
| ENST00000482438.2:n.98C>G | ||
| ENST00000494767.2:c.72C>G | ENSP00000489170.1:p.Leu24= | |
| ENST00000634359.1:n.198-191C>G | ||
| ENST00000634527.1:c.-318-191C>G | ENSP00000489039.1:n.-318-191C>G | |
| ENST00000634602.1:c.72C>G | ENSP00000489082.1:p.Leu24= | |
| ENST00000634609.1:n.97C>G | ||
| ENST00000634724.1:n.96C>G | ||
| ENST00000634802.1:c.72C>G | ENSP00000488917.1:p.Leu24= | |
| ENST00000634953.1:n.99C>G | ||
| ENST00000635052.1:c.72C>G | ENSP00000489409.1:p.Leu24= | |
| ENST00000635194.1:c.72C>G | ENSP00000488960.1:p.Leu24= | |
| ENST00000635231.1:c.72C>G | ENSP00000489550.1:p.Leu24= | |
| ENST00000635278.1:n.96C>G | ||
| ENST00000635443.1:c.72C>G | ENSP00000489154.1:p.Leu24= | |
| ENST00000635494.1:c.72C>G | ENSP00000489331.1:p.Leu24= | |
| ENST00000635501.1:n.462C>G | ||
| ENST00000635622.1:c.-392C>G | ENSP00000489558.1:n.-392C>G | |
| NM_001272073.1:c.72C>G | NP_001259002.1:p.Leu24= | |
| NM_005051.2:c.72C>G | NP_005042.1:p.Leu24= | |
| NR_073590.1:n.468C>G | ||
| XM_011533973.1:c.126C>G | XP_011532275.1:p.Leu42= | |
| XM_017006965.2:c.72C>G | XP_016862454.2:p.Leu24= | |
| NM_005051.3:c.72C>G MANE Select | NP_005042.1:p.Leu24= | |
| NM_001272073.2:c.72C>G | NP_001259002.1:p.Leu24= | |
| NR_073590.2:n.96C>G |