Linked Data
ClinVar Variation Id:
991618
ClinVar RCV Id:
RCV001279861
dbSNP Id:
rs1874730997
gnomAD v4:
12-102844327-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102844327A>C , CM000674.2:g.102844327A>C | GRCh38 |
| NC_000012.11:g.103238105A>C , CM000674.1:g.103238105A>C | GRCh37 |
| NC_000012.10:g.101762235A>C | NCBI36 |
| NG_008690.1:g.78276T>G | |
| NG_008690.2:g.119084T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000553106.6:c.1065+9T>G MANE Select | ENSP00000448059.1:n.1065+9T>G | |
| ENST00000307000.7:c.1050+9T>G | ENSP00000303500.2:n.1050+9T>G | |
| ENST00000549247.6:n.824+9T>G | ||
| ENST00000551114.2:n.727+9T>G | ||
| ENST00000553106.5:c.1065+9T>G | ENSP00000448059.1:n.1065+9T>G | |
| ENST00000635477.1:c.169+9T>G | ||
| ENST00000635528.1:n.580+9T>G | ||
| NM_000277.1:c.1065+9T>G | NP_000268.1:n.1065+9T>G | |
| XM_011538422.1:c.1008+9T>G | XP_011536724.1:n.1008+9T>G | |
| NM_000277.2:c.1065+9T>G | NP_000268.1:n.1065+9T>G | |
| NM_001354304.1:c.1065+9T>G | NP_001341233.1:n.1065+9T>G | |
| NM_000277.3:c.1065+9T>G MANE Select | NP_000268.1:n.1065+9T>G | |
| NM_001354304.2:c.1065+9T>G | NP_001341233.1:n.1065+9T>G |