Linked Data
MyVariant Identifiers:
chr10:g.124800129A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.123040613A>C , CM000672.2:g.123040613A>C | GRCh38 |
| NC_000010.10:g.124800129A>C , CM000672.1:g.124800129A>C | GRCh37 |
| NC_000010.9:g.124790119A>C | NCBI36 |
| NG_008003.1:g.36701A>C , LRG_451:g.36701A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000358776.7:c.451A>C MANE Select | ENSP00000357873.3:p.Arg151= | |
| ENST00000358776.6:c.451A>C | ENSP00000357873.3:p.Arg151= | |
| ENST00000368869.8:c.145A>C | ENSP00000357862.4:p.Arg49= | |
| ENST00000411816.2:n.468A>C | ||
| NM_001609.3:c.451A>C , LRG_451t1:c.451A>C | NP_001600.1:p.Arg151= | |
| NM_001330174.1:c.145A>C | NP_001317103.1:p.Arg49= | |
| NM_001330174.2:c.145A>C | NP_001317103.1:p.Arg49= | |
| NM_001609.4:c.451A>C MANE Select | NP_001600.1:p.Arg151= | |
| NM_001330174.3:c.145A>C | NP_001317103.1:p.Arg49= |