Linked Data
dbSNP Id:
rs1862865474
gnomAD v3:
12-7793095-A-G
gnomAD v4:
12-7793095-A-G
MyVariant Identifiers:
chr12:g.7945691A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.7793095A>G , CM000674.2:g.7793095A>G | GRCh38 |
| NC_000012.11:g.7945691A>G , CM000674.1:g.7945691A>G | GRCh37 |
| NC_000012.10:g.7836958A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000229307.9:c.297A>G MANE Select | ENSP00000229307.4:p.Arg99= | |
| ENST00000229307.8:c.297A>G | ENSP00000229307.4:p.Arg99= | |
| ENST00000526286.1:c.297A>G | ENSP00000435288.1:p.Arg99= | |
| ENST00000526434.2:n.441A>G | ||
| ENST00000541267.5:c.225A>G | ENSP00000444434.1:p.Arg75= | |
| NM_001297698.1:c.297A>G | NP_001284627.1:p.Arg99= | |
| NM_024865.3:c.297A>G | NP_079141.2:p.Arg99= | |
| XM_011520850.1:c.297A>G | XP_011519152.1:p.Arg99= | |
| XM_011520851.1:c.225A>G | XP_011519153.1:p.Arg75= | |
| XM_011520852.1:c.-76A>G | XP_011519154.1:n.-76A>G | |
| NM_024865.4:c.297A>G MANE Select | NP_079141.2:p.Arg99= | |
| NM_001297698.2:c.297A>G | NP_001284627.1:p.Arg99= |