Linked Data
MyVariant Identifiers:
chr10:g.96535148A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94775391A>C , CM000672.2:g.94775391A>C | GRCh38 |
| NC_000010.10:g.96535148A>C , CM000672.1:g.96535148A>C | GRCh37 |
| NC_000010.9:g.96525138A>C | NCBI36 |
| NG_008384.2:g.17686A>C | |
| NG_008384.3:g.17711A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000371321.9:c.333A>C MANE Select | ENSP00000360372.3:p.Gly111= | |
| ENST00000645461.1:n.1386A>C | ||
| ENST00000371321.7:c.333A>C | ENSP00000360372.3:p.Gly111= | |
| ENST00000464755.1:c.1096A>C | ENSP00000483243.1:n.1096A>C | |
| ENST00000480405.2:c.333A>C | ENSP00000483847.1:p.Gly111= | |
| NM_000769.2:c.333A>C | NP_000760.1:p.Gly111= | |
| NM_000769.4:c.333A>C MANE Select | NP_000760.1:p.Gly111= |