Linked Data
ClinVar Variation Id:
851685
ClinVar RCV Id:
RCV001056128
RCV001148001
RCV001148002
RCV001148003
RCV001149543
RCV002258114
RCV002482012
RCV004031776
dbSNP Id:
rs373819680
gnomAD v4:
3-122284503-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.122284503C>G , CM000665.2:g.122284503C>G | GRCh38 |
| NC_000003.11:g.122003350C>G , CM000665.1:g.122003350C>G | GRCh37 |
| NC_000003.10:g.123486040C>G | NCBI36 |
| NG_009058.1:g.105821C>G | |
| NG_009058.2:g.105836C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000490131.7:c.2318C>G | ENSP00000418685.2:p.Ala773Gly | |
| ENST00000498619.4:c.2579C>G | ENSP00000420194.1:p.Ala860Gly | |
| ENST00000638421.1:c.2549C>G | ENSP00000492190.1:p.Ala850Gly | |
| ENST00000639785.2:c.2549C>G MANE Select | ENSP00000491584.2:p.Ala850Gly | |
| ENST00000490131.5:c.2549C>G | ENSP00000418685.1:p.Ala850Gly | |
| ENST00000498619.2:c.2579C>G | ENSP00000420194.1:p.Ala860Gly | |
| NM_000388.3:c.2549C>G | NP_000379.2:p.Ala850Gly | |
| NM_001178065.1:c.2579C>G | NP_001171536.1:p.Ala860Gly | |
| XM_005247836.2:c.2549C>G | XP_005247893.1:p.Ala850Gly | |
| XM_005247837.2:c.2066C>G | XP_005247894.1:p.Ala689Gly | |
| XM_006713789.2:c.2549C>G | XP_006713852.1:p.Ala850Gly | |
| XM_011513237.1:c.2549C>G | XP_011511539.1:p.Ala850Gly | |
| XM_011513238.1:c.2549C>G | XP_011511540.1:p.Ala850Gly | |
| XM_011513239.1:c.1961C>G | XP_011511541.1:p.Ala654Gly | |
| XM_006713789.3:c.2549C>G | XP_006713852.1:p.Ala850Gly | |
| XM_017007324.1:c.2549C>G | XP_016862813.1:p.Ala850Gly | |
| XM_017007325.1:c.2549C>G | XP_016862814.1:p.Ala850Gly | |
| NM_000388.4:c.2549C>G MANE Select | NP_000379.3:p.Ala850Gly | |
| NM_001178065.2:c.2579C>G | NP_001171536.2:p.Ala860Gly |