Linked Data
ClinVar Variation Id:
1408962
ClinVar RCV Id:
RCV001913402
dbSNP Id:
rs1800908966
gnomAD v3:
4-122742977-A-G
gnomAD v4:
4-122742977-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.122742977A>G , CM000666.2:g.122742977A>G | GRCh38 |
| NC_000004.11:g.123664132A>G , CM000666.1:g.123664132A>G | GRCh37 |
| NC_000004.10:g.123883582A>G | NCBI36 |
| NG_021203.1:g.15276A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000314218.8:c.1085A>G MANE Select | ENSP00000319062.3:p.Asp362Gly | |
| ENST00000314218.7:c.1085A>G | ENSP00000319062.3:p.Asp362Gly | |
| ENST00000542236.5:c.1085A>G | ENSP00000438273.1:p.Asp362Gly | |
| NM_001178007.1:c.1085A>G | NP_001171478.1:p.Asp362Gly | |
| NM_152618.2:c.1085A>G | NP_689831.2:p.Asp362Gly | |
| XM_011531680.1:c.1085A>G | XP_011529982.1:p.Asp362Gly | |
| XM_011531680.2:c.1085A>G | XP_011529982.1:p.Asp362Gly | |
| XM_017007831.1:c.1085A>G | XP_016863320.1:p.Asp362Gly | |
| NM_152618.3:c.1085A>G MANE Select | NP_689831.2:p.Asp362Gly | |
| NM_001178007.2:c.1085A>G | NP_001171478.1:p.Asp362Gly |