Linked Data
dbSNP Id:
rs1948143462
gnomAD v3:
11-118312820-A-G
gnomAD v4:
11-118312820-A-G
MyVariant Identifiers:
chr11:g.118183535A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.118312820A>G , CM000673.2:g.118312820A>G | GRCh38 |
| NC_000011.9:g.118183535A>G , CM000673.1:g.118183535A>G | GRCh37 |
| NC_000011.8:g.117688745A>G | NCBI36 |
| NG_007383.1:g.13241A>G , LRG_38:g.13241A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361763.9:c.306A>G MANE Select | ENSP00000354566.4:p.Gly102= | |
| ENST00000361763.8:c.306A>G | ENSP00000354566.4:p.Gly102= | |
| ENST00000526146.5:n.852A>G | ||
| ENST00000528435.5:n.859A>G | ||
| ENST00000528600.1:c.288A>G | ENSP00000433975.1:p.Gly96= | |
| ENST00000529713.5:n.412A>G | ||
| ENST00000531913.1:n.677A>G | ||
| NM_000733.3:c.306A>G , LRG_38t1:c.306A>G | NP_000724.1:p.Gly102= | |
| NM_000733.4:c.306A>G MANE Select | NP_000724.1:p.Gly102= |