Linked Data
ClinVar Variation Id:
554266
ClinVar RCV Id:
RCV001526923
dbSNP Id:
rs63329263
gnomAD v4:
12-102843756-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102843756C>G , CM000674.2:g.102843756C>G | GRCh38 |
| NC_000012.11:g.103237534C>G , CM000674.1:g.103237534C>G | GRCh37 |
| NC_000012.10:g.101761664C>G | NCBI36 |
| NG_008690.1:g.78847G>C | |
| NG_008690.2:g.119655G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000553106.6:c.1089G>C MANE Select | ENSP00000448059.1:p.Lys363Asn | |
| ENST00000307000.7:c.1074G>C | ENSP00000303500.2:p.Lys358Asn | |
| ENST00000549247.6:n.848G>C | ||
| ENST00000551114.2:n.751G>C | ||
| ENST00000553106.5:c.1089G>C | ENSP00000448059.1:p.Lys363Asn | |
| ENST00000635477.1:c.193G>C | ||
| ENST00000635528.1:n.604G>C | ||
| NM_000277.1:c.1089G>C | NP_000268.1:p.Lys363Asn | |
| XM_011538422.1:c.1032G>C | XP_011536724.1:p.Lys344Asn | |
| NM_000277.2:c.1089G>C | NP_000268.1:p.Lys363Asn | |
| NM_001354304.1:c.1089G>C | NP_001341233.1:p.Lys363Asn | |
| NM_000277.3:c.1089G>C MANE Select | NP_000268.1:p.Lys363Asn | |
| NM_001354304.2:c.1089G>C | NP_001341233.1:p.Lys363Asn |