Linked Data
ClinVar Variation Id:
40177
ClinVar RCV Id:
RCV000033199
dbSNP Id:
rs397515435
ExAC:
2:26703836 C / T
gnomAD v2:
2-26703836-C-T
gnomAD v4:
2-26480968-C-T
PubMed:
PMID:22575033
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.26480968C>T , CM000664.2:g.26480968C>T | GRCh38 |
| NC_000002.11:g.26703836C>T , CM000664.1:g.26703836C>T | GRCh37 |
| NC_000002.10:g.26557340C>T | NCBI36 |
| NG_009937.1:g.82731G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000272371.7:c.1621G>A MANE Select | ENSP00000272371.2:p.Gly541Ser | |
| ENST00000272371.6:c.1621G>A | ENSP00000272371.2:p.Gly541Ser | |
| ENST00000403946.7:c.1621G>A | ENSP00000385255.3:p.Gly541Ser | |
| NM_001287489.1:c.1621G>A | NP_001274418.1:p.Gly541Ser | |
| NM_194248.2:c.1621G>A | NP_919224.1:p.Gly541Ser | |
| XM_005264644.2:c.1666G>A | XP_005264701.1:p.Gly556Ser | |
| XM_011533185.1:c.1666G>A | XP_011531487.1:p.Gly556Ser | |
| XM_017005338.1:c.1621G>A | XP_016860827.1:p.Gly541Ser | |
| NM_001287489.2:c.1621G>A | NP_001274418.1:p.Gly541Ser | |
| NM_194248.3:c.1621G>A MANE Select | NP_919224.1:p.Gly541Ser |