Linked Data
ClinVar Variation Id:
201694
dbSNP Id:
rs746207
ExAC:
11:19209735 C / A
gnomAD v2:
11-19209735-C-A
gnomAD v4:
11-19188188-C-A
COSMIC:
COSM388972
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.19188188C>A , CM000673.2:g.19188188C>A | GRCh38 |
| NC_000011.9:g.19209735C>A , CM000673.1:g.19209735C>A | GRCh37 |
| NC_000011.8:g.19166311C>A | NCBI36 |
| NG_011932.2:g.27386G>T , LRG_440:g.27386G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265968.9:c.229G>T MANE Select | ENSP00000265968.3:p.Ala77Ser | |
| ENST00000533783.2:c.229G>T | ENSP00000431813.1:p.Ala77Ser | |
| ENST00000647990.1:c.229G>T | ENSP00000496798.1:p.Ala77Ser | |
| ENST00000648719.1:c.113-3143G>T | ENSP00000497633.1:n.113-3143G>T | |
| ENST00000649235.1:c.229G>T | ENSP00000497388.1:p.Ala77Ser | |
| ENST00000649842.1:c.113-1840G>T | ENSP00000497531.1:n.113-1840G>T | |
| ENST00000265968.7:c.229G>T | ENSP00000265968.3:p.Ala77Ser | |
| ENST00000533783.1:c.229G>T | ENSP00000431813.1:p.Ala77Ser | |
| NM_003476.4:c.229G>T | NP_003467.1:p.Ala77Ser | |
| XM_024448698.1:c.113-1840G>T | XP_024304466.1:n.113-1840G>T | |
| NM_001369404.1:c.113-1840G>T | NP_001356333.1:n.113-1840G>T | |
| NM_003476.5:c.229G>T MANE Select | NP_003467.1:p.Ala77Ser |