Linked Data
ClinVar Variation Id:
264121
dbSNP Id:
rs775987665
gnomAD v3:
5-128335259-T-C
gnomAD v4:
5-128335259-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.128335259T>C , CM000667.2:g.128335259T>C | GRCh38 |
| NC_000005.9:g.127670951T>C , CM000667.1:g.127670951T>C | GRCh37 |
| NC_000005.8:g.127698850T>C | NCBI36 |
| NG_008750.1:g.207785A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000703783.1:n.668A>G | ||
| ENST00000703785.1:n.749A>G | ||
| ENST00000262464.9:c.3884A>G MANE Select | ENSP00000262464.4:p.Asp1295Gly | |
| ENST00000262464.8:c.3884A>G | ENSP00000262464.4:p.Asp1295Gly | |
| ENST00000507835.5:c.434A>G | ENSP00000426839.1:p.Asp145Gly | |
| ENST00000508053.5:c.3884A>G | ENSP00000424571.1:p.Asp1295Gly | |
| ENST00000508989.5:c.3785A>G | ENSP00000425596.1:p.Asp1262Gly | |
| ENST00000619499.4:c.3881A>G | ENSP00000482132.1:p.Asp1294Gly | |
| NM_001999.3:c.3884A>G | NP_001990.2:p.Asp1295Gly | |
| XM_017009228.2:c.3731A>G | XP_016864717.1:p.Asp1244Gly | |
| NM_001999.4:c.3884A>G MANE Select | NP_001990.2:p.Asp1295Gly |