Linked Data
MyVariant Identifiers:
chr15:g.23889587C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.23644440C>A , CM000677.2:g.23644440C>A | GRCh38 |
| NC_000015.9:g.23889587C>A , CM000677.1:g.23889587C>A | GRCh37 |
| NC_000015.8:g.21440680C>A | NCBI36 |
| NG_016776.1:g.8407G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650528.1:c.3303G>T MANE Select | ENSP00000497810.1:p.Val1101= | |
| ENST00000532292.2:c.3303G>T | ENSP00000433433.2:p.Val1101= | |
| NM_019066.4:c.3303G>T | NP_061939.3:p.Val1101= | |
| NM_019066.5:c.3303G>T MANE Select | NP_061939.3:p.Val1101= |