Linked Data
ClinVar Variation Id:
40498
dbSNP Id:
rs397507511
ExAC:
12:112888189 G / C
COSMIC:
COSM6006328
ERepo:
CA261565/MONDO:0021060/004
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.112450385G>C , CM000674.2:g.112450385G>C | GRCh38 |
| NC_000012.11:g.112888189G>C , CM000674.1:g.112888189G>C | GRCh37 |
| NC_000012.10:g.111372572G>C | NCBI36 |
| NG_007459.1:g.36654G>C , LRG_614:g.36654G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000639857.2:c.205G>C | ENSP00000491593.2:p.Glu69Gln | |
| ENST00000685487.1:c.205G>C | ENSP00000508503.1:p.Glu69Gln | |
| ENST00000687906.1:c.205G>C | ENSP00000509536.1:p.Glu69Gln | |
| ENST00000688597.1:c.205G>C | ENSP00000510628.1:p.Glu69Gln | |
| ENST00000690210.1:c.205G>C | ENSP00000509272.1:p.Glu69Gln | |
| ENST00000692624.1:c.205G>C | ENSP00000508953.1:p.Glu69Gln | |
| ENST00000351677.7:c.205G>C MANE Select | ENSP00000340944.3:p.Glu69Gln | |
| ENST00000639857.1:c.205G>C | ENSP00000491593.1:p.Glu69Gln | |
| ENST00000351677.6:c.205G>C | ENSP00000340944.2:p.Glu69Gln | |
| ENST00000392597.5:c.205G>C | ENSP00000376376.1:p.Glu69Gln | |
| ENST00000635625.1:c.205G>C | ENSP00000489597.1:p.Glu69Gln | |
| NM_002834.3:c.205G>C , LRG_614t1:c.205G>C | NP_002825.3:p.Glu69Gln | |
| NM_080601.1:c.205G>C | NP_542168.1:p.Glu69Gln | |
| XM_006719526.1:c.205G>C | XP_006719589.1:p.Glu69Gln | |
| XM_006719527.1:c.205G>C | XP_006719590.1:p.Glu69Gln | |
| XM_011538613.1:c.202G>C | XP_011536915.1:p.Glu68Gln | |
| NM_001330437.1:c.205G>C | NP_001317366.1:p.Glu69Gln | |
| NM_002834.4:c.205G>C | NP_002825.3:p.Glu69Gln | |
| NM_080601.2:c.205G>C | NP_542168.1:p.Glu69Gln | |
| XM_011538613.2:c.202G>C | XP_011536915.1:p.Glu68Gln | |
| XM_017019722.1:c.202G>C | XP_016875211.1:p.Glu68Gln | |
| NM_001330437.2:c.205G>C | NP_001317366.1:p.Glu69Gln | |
| NM_001374625.1:c.202G>C | NP_001361554.1:p.Glu68Gln | |
| NM_002834.5:c.205G>C MANE Select | NP_002825.3:p.Glu69Gln | |
| NM_080601.3:c.205G>C | NP_542168.1:p.Glu69Gln |