Linked Data
MyVariant Identifiers:
chr15:g.23889614C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.23644467C>T , CM000677.2:g.23644467C>T | GRCh38 |
| NC_000015.9:g.23889614C>T , CM000677.1:g.23889614C>T | GRCh37 |
| NC_000015.8:g.21440707C>T | NCBI36 |
| NG_016776.1:g.8380G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650528.1:c.3276G>A MANE Select | ENSP00000497810.1:p.Lys1092= | |
| ENST00000532292.2:c.3276G>A | ENSP00000433433.2:p.Lys1092= | |
| NM_019066.4:c.3276G>A | NP_061939.3:p.Lys1092= | |
| NM_019066.5:c.3276G>A MANE Select | NP_061939.3:p.Lys1092= |