Linked Data
ClinVar Variation Id:
2773077
ClinVar RCV Id:
RCV003577000
gnomAD v4:
11-18287561-C-G
MyVariant Identifiers:
chr11:g.18309108C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.18287561C>G , CM000673.2:g.18287561C>G | GRCh38 |
| NC_000011.9:g.18309108C>G , CM000673.1:g.18309108C>G | GRCh37 |
| NC_000011.8:g.18265684C>G | NCBI36 |
| NG_008877.1:g.39614G>C , LRG_586:g.39614G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000349215.8:c.2691G>C MANE Select | ENSP00000265967.5:p.Leu897= | |
| ENST00000349215.7:c.2691G>C | ENSP00000265967.5:p.Leu897= | |
| ENST00000352460.7:n.1082G>C | ||
| ENST00000396253.7:c.2349G>C | ENSP00000379552.3:p.Leu783= | |
| ENST00000438420.6:c.2349G>C | ENSP00000399590.2:p.Leu783= | |
| ENST00000544218.5:c.249G>C | ENSP00000441781.1:p.Leu83= | |
| ENST00000545561.1:n.752G>C | ||
| NM_007216.3:c.2349G>C | NP_009147.3:p.Leu783= | |
| NM_181507.1:c.2691G>C , LRG_586t1:c.2691G>C | NP_852608.1:p.Leu897= | |
| NM_181508.1:c.2349G>C | NP_852609.1:p.Leu783= | |
| XM_011519862.1:c.2691G>C | XP_011518164.1:p.Leu897= | |
| XM_011519863.1:c.2691G>C | XP_011518165.1:p.Leu897= | |
| XM_011519864.1:c.2691G>C | XP_011518166.1:p.Leu897= | |
| XM_011519865.1:c.2580G>C | XP_011518167.1:p.Leu860= | |
| XM_011519866.1:c.2349G>C | XP_011518168.1:p.Leu783= | |
| XM_011519867.1:c.2349G>C | XP_011518169.1:p.Leu783= | |
| XM_011519868.1:c.2349G>C | XP_011518170.1:p.Leu783= | |
| XM_011519869.1:c.2691G>C | XP_011518171.1:p.Leu897= | |
| XM_011519870.1:c.*175G>C | XP_011518172.1:n.*175G>C | |
| XM_011519871.1:c.*175G>C | XP_011518173.1:n.*175G>C | |
| XM_011519868.3:c.2349G>C | XP_011518170.1:p.Leu783= | |
| XM_017017149.1:c.2691G>C | XP_016872638.1:p.Leu897= | |
| XM_017017150.1:c.2691G>C | XP_016872639.1:p.Leu897= | |
| XM_017017151.2:c.2580G>C | XP_016872640.1:p.Leu860= | |
| XM_017017152.1:c.2580G>C | XP_016872641.1:p.Leu860= | |
| XM_017017153.2:c.2580G>C | XP_016872642.1:p.Leu860= | |
| XM_017017154.1:c.2349G>C | XP_016872643.1:p.Leu783= | |
| XR_001747750.1:n.2960G>C | ||
| XR_001747751.1:n.2960G>C | ||
| XR_001747752.1:n.2716G>C | ||
| XR_001747753.1:n.2833G>C | ||
| XR_001747754.2:n.2357G>C | ||
| XR_001747755.2:n.2279G>C | ||
| XR_001747756.2:n.2292G>C | ||
| NM_007216.4:c.2349G>C | NP_009147.3:p.Leu783= | |
| NM_181507.2:c.2691G>C MANE Select | NP_852608.1:p.Leu897= |