Linked Data
ClinVar Variation Id:
2919786
ClinVar RCV Id:
RCV003753873
gnomAD v4:
12-51688821-G-A
MyVariant Identifiers:
chr12:g.52082605G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.51688821G>A , CM000674.2:g.51688821G>A | GRCh38 |
| NC_000012.11:g.52082605G>A , CM000674.1:g.52082605G>A | GRCh37 |
| NC_000012.10:g.50368872G>A | NCBI36 |
| NG_021180.2:g.102586G>A | |
| NG_021180.3:g.103864G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000703687.1:n.2445G>A | ||
| ENST00000354534.11:c.678G>A MANE Plus Clinical | ENSP00000346534.4:p.Arg226= | |
| ENST00000627620.5:c.615-184G>A MANE Select | ENSP00000487583.2:n.615-184G>A | |
| ENST00000637709.2:c.678G>A | ENSP00000490470.1:p.Arg226= | |
| ENST00000638820.1:c.615-184G>A | ENSP00000492157.1:n.615-184G>A | |
| ENST00000662684.1:c.615-184G>A | ENSP00000499636.1:n.615-184G>A | |
| ENST00000667214.1:c.678G>A | ENSP00000499724.1:p.Arg226= | |
| ENST00000668547.1:c.615-184G>A | ENSP00000499691.1:n.615-184G>A | |
| ENST00000354534.10:c.678G>A | ENSP00000346534.4:p.Arg226= | |
| ENST00000355133.7:c.678G>A | ENSP00000347255.4:p.Arg226= | |
| ENST00000545061.5:c.678G>A | ENSP00000440360.1:p.Arg226= | |
| ENST00000550891.4:n.743-184G>A | ||
| ENST00000551216.2:c.165-184G>A | ENSP00000447567.2:n.165-184G>A | |
| ENST00000599343.5:c.678G>A | ENSP00000476447.3:p.Arg226= | |
| ENST00000627620.2:c.615-184G>A | ENSP00000487583.1:n.615-184G>A | |
| NM_001177984.2:c.678G>A | NP_001171455.1:p.Arg226= | |
| NM_014191.3:c.678G>A | NP_055006.1:p.Arg226= | |
| XM_006719556.2:c.615-184G>A | XP_006719619.1:n.615-184G>A | |
| XM_011538650.1:c.615-184G>A | XP_011536952.1:n.615-184G>A | |
| XM_011538651.1:c.615-184G>A | XP_011536953.1:n.615-184G>A | |
| NM_001330260.1:c.615-184G>A | NP_001317189.1:n.615-184G>A | |
| XM_006719556.4:c.615-184G>A | XP_006719619.1:n.615-184G>A | |
| XM_011538651.3:c.615-184G>A | XP_011536953.1:n.615-184G>A | |
| XM_017019794.2:c.678G>A | XP_016875283.1:p.Arg226= | |
| XM_017019795.2:c.615-184G>A | XP_016875284.1:n.615-184G>A | |
| XM_017019796.1:c.615-184G>A | XP_016875285.1:n.615-184G>A | |
| NM_001330260.2:c.615-184G>A MANE Select | NP_001317189.1:n.615-184G>A | |
| NM_001369788.1:c.615-184G>A | NP_001356717.1:n.615-184G>A | |
| NM_014191.4:c.678G>A MANE Plus Clinical | NP_055006.1:p.Arg226= | |
| NM_001177984.3:c.678G>A | NP_001171455.1:p.Arg226= |