Linked Data
ClinVar Variation Id:
2788448
ClinVar RCV Id:
RCV003633892
MyVariant Identifiers:
chr2:g.32288987G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.32063918G>A , CM000664.2:g.32063918G>A | GRCh38 |
| NC_000002.11:g.32288987G>A , CM000664.1:g.32288987G>A | GRCh37 |
| NC_000002.10:g.32142491G>A | NCBI36 |
| NG_008730.1:g.5308G>A , LRG_714:g.5308G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000704289.1:c.87G>A | ENSP00000515816.1:p.Leu29= | |
| ENST00000315285.9:c.87G>A MANE Select | ENSP00000320885.3:p.Leu29= | |
| ENST00000621856.2:c.87G>A | ENSP00000482496.2:p.Leu29= | |
| ENST00000642455.1:c.87G>A | ENSP00000493827.1:p.Leu29= | |
| ENST00000646571.1:c.87G>A | ENSP00000495015.1:p.Leu29= | |
| ENST00000315285.7:c.87G>A | ENSP00000320885.3:p.Leu29= | |
| ENST00000345662.5:c.87G>A | ENSP00000340817.1:p.Leu29= | |
| ENST00000615843.4:c.87G>A | ENSP00000480893.1:p.Leu29= | |
| NM_014946.3:c.87G>A , LRG_714t1:c.87G>A | NP_055761.2:p.Leu29= | |
| NM_199436.1:c.87G>A | NP_955468.1:p.Leu29= | |
| XM_005264516.3:c.87G>A | XP_005264573.1:p.Leu29= | |
| XM_011533067.1:c.87G>A | XP_011531369.1:p.Leu29= | |
| NM_001363823.1:c.87G>A | NP_001350752.1:p.Leu29= | |
| NM_001363875.1:c.87G>A | NP_001350804.1:p.Leu29= | |
| XM_005264516.5:c.87G>A | XP_005264573.1:p.Leu29= | |
| XM_011533067.2:c.87G>A | XP_011531369.1:p.Leu29= | |
| XM_017004778.2:c.87G>A | XP_016860267.1:p.Leu29= | |
| NM_001363823.2:c.87G>A | NP_001350752.1:p.Leu29= | |
| NM_001363875.2:c.87G>A | NP_001350804.1:p.Leu29= | |
| NM_001377959.1:c.87G>A | NP_001364888.1:p.Leu29= | |
| NM_014946.4:c.87G>A MANE Select | NP_055761.2:p.Leu29= | |
| NM_199436.2:c.87G>A | NP_955468.1:p.Leu29= |