Linked Data
dbSNP Id:
rs373048216
gnomAD v4:
10-94981307-C-A
MyVariant Identifiers:
chr10:g.96741064C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94981307C>A , CM000672.2:g.94981307C>A | GRCh38 |
| NC_000010.10:g.96741064C>A , CM000672.1:g.96741064C>A | GRCh37 |
| NC_000010.9:g.96731054C>A | NCBI36 |
| NG_008385.1:g.47650C>A | |
| NG_008385.2:g.48150C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000260682.8:c.1086C>A MANE Select | ENSP00000260682.6:p.Leu362= | |
| ENST00000643112.1:c.*95C>A | ENSP00000496202.1:n.*95C>A | |
| ENST00000260682.6:c.1086C>A | ENSP00000260682.6:p.Leu362= | |
| NM_000771.3:c.1086C>A | NP_000762.2:p.Leu362= | |
| NM_000771.4:c.1086C>A MANE Select | NP_000762.2:p.Leu362= |