Linked Data
dbSNP Id:
rs2032364780
gnomAD v4:
10-94988869-A-G
MyVariant Identifiers:
chr10:g.96748626A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94988869A>G , CM000672.2:g.94988869A>G | GRCh38 |
| NC_000010.10:g.96748626A>G , CM000672.1:g.96748626A>G | GRCh37 |
| NC_000010.9:g.96738616A>G | NCBI36 |
| NG_008385.1:g.55212A>G | |
| NG_008385.2:g.55712A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260682.8:c.1314A>G MANE Select | ENSP00000260682.6:p.Glu438= | |
| ENST00000643112.1:c.*323A>G | ENSP00000496202.1:n.*323A>G | |
| ENST00000260682.6:c.1314A>G | ENSP00000260682.6:p.Glu438= | |
| NM_000771.3:c.1314A>G | NP_000762.2:p.Glu438= | |
| NM_000771.4:c.1314A>G MANE Select | NP_000762.2:p.Glu438= |