Linked Data
MyVariant Identifiers:
chr10:g.96701968A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94942211A>C , CM000672.2:g.94942211A>C | GRCh38 |
| NC_000010.10:g.96701968A>C , CM000672.1:g.96701968A>C | GRCh37 |
| NC_000010.9:g.96691958A>C | NCBI36 |
| NG_008385.1:g.8554A>C | |
| NG_008385.2:g.9054A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000260682.8:c.351A>C MANE Select | ENSP00000260682.6:p.Gly117= | |
| ENST00000643112.1:c.351A>C | ENSP00000496202.1:p.Gly117= | |
| ENST00000645207.1:n.504A>C | ||
| ENST00000260682.6:c.351A>C | ENSP00000260682.6:p.Gly117= | |
| ENST00000461906.1:n.376A>C | ||
| ENST00000473496.1:n.122A>C | ||
| NM_000771.3:c.351A>C | NP_000762.2:p.Gly117= | |
| NM_000771.4:c.351A>C MANE Select | NP_000762.2:p.Gly117= |