Linked Data
dbSNP Id:
rs2140397608
gnomAD v3:
12-57766024-A-G
gnomAD v4:
12-57766024-A-G
MyVariant Identifiers:
chr12:g.58159807A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57766024A>G , CM000674.2:g.57766024A>G | GRCh38 |
| NC_000012.11:g.58159807A>G , CM000674.1:g.58159807A>G | GRCh37 |
| NC_000012.10:g.56446074A>G | NCBI36 |
| NG_007076.1:g.6170T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000546609.2:n.281T>C | ||
| ENST00000713544.1:c.369T>C | ENSP00000518840.1:p.Ala123= | |
| ENST00000713545.1:c.369T>C | ENSP00000518841.1:p.Ala123= | |
| ENST00000228606.9:c.369T>C MANE Select | ENSP00000228606.4:p.Ala123= | |
| ENST00000228606.8:c.369T>C | ENSP00000228606.4:p.Ala123= | |
| ENST00000546496.1:n.197T>C | ||
| ENST00000546609.1:c.281T>C | ||
| ENST00000547344.5:n.423T>C | ||
| ENST00000552186.1:n.488T>C | ||
| NM_000785.3:c.369T>C | NP_000776.1:p.Ala123= | |
| NM_000785.4:c.369T>C MANE Select | NP_000776.1:p.Ala123= |