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