Linked Data
ClinVar Variation Id:
3026880
ClinVar RCV Id:
RCV003887273
gnomAD v4:
5-149978060-A-G
MyVariant Identifiers:
chr5:g.149357623A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.149978060A>G , CM000667.2:g.149978060A>G | GRCh38 |
| NC_000005.9:g.149357623A>G , CM000667.1:g.149357623A>G | GRCh37 |
| NC_000005.8:g.149337816A>G | NCBI36 |
| NG_007147.2:g.19178A>G , LRG_684:g.19178A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000690410.1:n.640A>G | ||
| ENST00000286298.5:c.408A>G MANE Select | ENSP00000286298.4:p.Glu136= | |
| ENST00000286298.4:c.408A>G | ENSP00000286298.4:p.Glu136= | |
| ENST00000503336.1:c.81A>G | ENSP00000426053.1:p.Glu27= | |
| NM_000112.3:c.408A>G , LRG_684t1:c.408A>G | NP_000103.2:p.Glu136= | |
| XM_017009191.2:c.408A>G | XP_016864680.1:p.Glu136= | |
| NM_000112.4:c.408A>G MANE Select | NP_000103.2:p.Glu136= |