Linked Data
MyVariant Identifiers:
chr10:g.96740965T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94981208T>C , CM000672.2:g.94981208T>C | GRCh38 |
| NC_000010.10:g.96740965T>C , CM000672.1:g.96740965T>C | GRCh37 |
| NC_000010.9:g.96730955T>C | NCBI36 |
| NG_008385.1:g.47551T>C | |
| NG_008385.2:g.48051T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000260682.8:c.987T>C MANE Select | ENSP00000260682.6:p.Arg329= | |
| ENST00000643112.1:c.845T>C | ENSP00000496202.1:p.Val282Ala | |
| ENST00000260682.6:c.987T>C | ENSP00000260682.6:p.Arg329= | |
| NM_000771.3:c.987T>C | NP_000762.2:p.Arg329= | |
| NM_000771.4:c.987T>C MANE Select | NP_000762.2:p.Arg329= |