Linked Data
MyVariant Identifiers:
chr10:g.96612623A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94852866A>C , CM000672.2:g.94852866A>C | GRCh38 |
| NC_000010.10:g.96612623A>C , CM000672.1:g.96612623A>C | GRCh37 |
| NC_000010.9:g.96602613A>C | NCBI36 |
| NG_008384.2:g.95161A>C | |
| NG_008384.3:g.95186A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371321.9:c.1425A>C MANE Select | ENSP00000360372.3:p.Gly475= | |
| ENST00000645461.1:n.2336A>C | ||
| ENST00000371321.7:c.1425A>C | ENSP00000360372.3:p.Gly475= | |
| ENST00000464755.1:c.2188A>C | ENSP00000483243.1:n.2188A>C | |
| NM_000769.2:c.1425A>C | NP_000760.1:p.Gly475= | |
| NM_000769.4:c.1425A>C MANE Select | NP_000760.1:p.Gly475= |