Linked Data
ClinVar Variation Id:
21855
ClinVar RCV Id:
RCV000021066
dbSNP Id:
rs80356579
PubMed:
PMID:20301429
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.26464956C>T , CM000664.2:g.26464956C>T | GRCh38 |
| NC_000002.11:g.26687824C>T , CM000664.1:g.26687824C>T | GRCh37 |
| NC_000002.10:g.26541328C>T | NCBI36 |
| NG_009937.1:g.98743G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000272371.7:c.4873G>A MANE Select | ENSP00000272371.2:p.Val1625Met | |
| ENST00000339598.8:c.2572G>A MANE Plus Clinical | ENSP00000344521.3:p.Val858Met | |
| ENST00000402415.8:c.2632G>A | ENSP00000383906.4:p.Val878Met | |
| ENST00000272371.6:c.4873G>A | ENSP00000272371.2:p.Val1625Met | |
| ENST00000338581.10:c.2572G>A | ENSP00000345137.6:p.Val858Met | |
| ENST00000339598.7:c.2572G>A | ENSP00000344521.3:p.Val858Met | |
| ENST00000402415.7:c.2803G>A | ENSP00000383906.3:p.Val935Met | |
| ENST00000403946.7:c.4873G>A | ENSP00000385255.3:p.Val1625Met | |
| ENST00000464574.1:n.622G>A | ||
| NM_001287489.1:c.4873G>A | NP_001274418.1:p.Val1625Met | |
| NM_004802.3:c.2572G>A | NP_004793.2:p.Val858Met | |
| NM_194248.2:c.4873G>A | NP_919224.1:p.Val1625Met | |
| NM_194322.2:c.2803G>A | NP_919303.1:p.Val935Met | |
| NM_194323.2:c.2572G>A | NP_919304.1:p.Val858Met | |
| XM_005264644.2:c.4858G>A | XP_005264701.1:p.Val1620Met | |
| XM_011533185.1:c.4918G>A | XP_011531487.1:p.Val1640Met | |
| XM_017005338.1:c.4813G>A | XP_016860827.1:p.Val1605Met | |
| NM_001287489.2:c.4873G>A | NP_001274418.1:p.Val1625Met | |
| NM_004802.4:c.2572G>A | NP_004793.2:p.Val858Met | |
| NM_194248.3:c.4873G>A MANE Select | NP_919224.1:p.Val1625Met | |
| NM_194322.3:c.2803G>A | NP_919303.1:p.Val935Met | |
| NM_194323.3:c.2572G>A MANE Plus Clinical | NP_919304.1:p.Val858Met |