Linked Data
MyVariant Identifiers:
chr10:g.115804152G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.114044393G>C , CM000672.2:g.114044393G>C | GRCh38 |
| NC_000010.10:g.115804152G>C , CM000672.1:g.115804152G>C | GRCh37 |
| NC_000010.9:g.115794142G>C | NCBI36 |
| NG_012187.1:g.5347G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369295.4:c.261G>C MANE Select | ENSP00000358301.2:p.Pro87= | |
| ENST00000369295.3:c.261G>C | ENSP00000358301.2:p.Pro87= | |
| NM_000684.2:c.261G>C | NP_000675.1:p.Pro87= | |
| NM_000684.3:c.261G>C MANE Select | NP_000675.1:p.Pro87= |