Linked Data
ClinVar Variation Id:
2933006
ClinVar RCV Id:
RCV003798172
gnomAD v4:
12-101786067-T-C
MyVariant Identifiers:
chr12:g.102179845T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.101786067T>C , CM000674.2:g.101786067T>C | GRCh38 |
| NC_000012.11:g.102179845T>C , CM000674.1:g.102179845T>C | GRCh37 |
| NC_000012.10:g.100703976T>C | NCBI36 |
| NG_021243.1:g.49801A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000299314.12:c.516A>G MANE Select | ENSP00000299314.7:p.Lys172= | |
| ENST00000299314.11:c.516A>G | ENSP00000299314.7:p.Lys172= | |
| ENST00000549940.5:c.516A>G | ENSP00000449150.1:p.Lys172= | |
| ENST00000550352.1:n.310A>G | ||
| ENST00000552681.1:c.150A>G | ENSP00000449217.1:p.Lys50= | |
| NM_024312.4:c.516A>G | NP_077288.2:p.Lys172= | |
| XM_006719593.2:c.516A>G | XP_006719656.1:p.Lys172= | |
| XM_011538731.1:c.435A>G | XP_011537033.1:p.Lys145= | |
| XM_006719593.3:c.516A>G | XP_006719656.1:p.Lys172= | |
| XM_011538731.2:c.435A>G | XP_011537033.1:p.Lys145= | |
| XM_017019961.1:c.300A>G | XP_016875450.1:p.Lys100= | |
| XM_017019962.2:c.-835A>G | XP_016875451.1:n.-835A>G | |
| NM_024312.5:c.516A>G MANE Select | NP_077288.2:p.Lys172= |