Linked Data
ClinVar Variation Id:
213379
dbSNP Id:
rs146941428
gnomAD v2:
5-127800510-G-A
gnomAD v3:
5-128464817-G-A
gnomAD v4:
5-128464817-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.128464817G>A , CM000667.2:g.128464817G>A | GRCh38 |
| NC_000005.9:g.127800510G>A , CM000667.1:g.127800510G>A | GRCh37 |
| NC_000005.8:g.127828409G>A | NCBI36 |
| NG_008750.1:g.78226C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000508053.6:c.733C>T | ENSP00000424571.2:p.Arg245Trp | |
| ENST00000703787.1:n.440C>T | ||
| ENST00000262464.9:c.733C>T MANE Select | ENSP00000262464.4:p.Arg245Trp | |
| ENST00000262464.8:c.733C>T | ENSP00000262464.4:p.Arg245Trp | |
| ENST00000502468.5:c.733C>T | ENSP00000424753.1:p.Arg245Trp | |
| ENST00000508053.5:c.733C>T | ENSP00000424571.1:p.Arg245Trp | |
| ENST00000508989.5:c.634C>T | ENSP00000425596.1:p.Arg212Trp | |
| ENST00000514742.1:n.1353C>T | ||
| ENST00000619499.4:c.730C>T | ENSP00000482132.1:p.Arg244Trp | |
| ENST00000620257.1:c.733C>T | ENSP00000479157.1:p.Arg245Trp | |
| NM_001999.3:c.733C>T | NP_001990.2:p.Arg245Trp | |
| XM_017009228.2:c.733C>T | XP_016864717.1:p.Arg245Trp | |
| NM_001999.4:c.733C>T MANE Select | NP_001990.2:p.Arg245Trp |