Linked Data
ClinVar Variation Id:
2015351
ClinVar RCV Id:
RCV002839409
dbSNP Id:
rs201316578
MyVariant Identifiers:
chr12:g.102179910G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.101786132G>A , CM000674.2:g.101786132G>A | GRCh38 |
| NC_000012.11:g.102179910G>A , CM000674.1:g.102179910G>A | GRCh37 |
| NC_000012.10:g.100704041G>A | NCBI36 |
| NG_021243.1:g.49736C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000299314.12:c.451C>T MANE Select | ENSP00000299314.7:p.Leu151= | |
| ENST00000299314.11:c.451C>T | ENSP00000299314.7:p.Leu151= | |
| ENST00000549940.5:c.451C>T | ENSP00000449150.1:p.Leu151= | |
| ENST00000550352.1:n.245C>T | ||
| ENST00000552681.1:c.85C>T | ENSP00000449217.1:p.Leu29= | |
| NM_024312.4:c.451C>T | NP_077288.2:p.Leu151= | |
| XM_006719593.2:c.451C>T | XP_006719656.1:p.Leu151= | |
| XM_011538731.1:c.370C>T | XP_011537033.1:p.Leu124= | |
| XM_006719593.3:c.451C>T | XP_006719656.1:p.Leu151= | |
| XM_011538731.2:c.370C>T | XP_011537033.1:p.Leu124= | |
| XM_017019961.1:c.235C>T | XP_016875450.1:p.Leu79= | |
| XM_017019962.2:c.-900C>T | XP_016875451.1:n.-900C>T | |
| NM_024312.5:c.451C>T MANE Select | NP_077288.2:p.Leu151= |