Linked Data
dbSNP Id:
rs868741666
gnomAD v2:
11-69464819-C-T
gnomAD v3:
11-69650051-C-T
gnomAD v4:
11-69650051-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.69650051C>T , CM000673.2:g.69650051C>T | GRCh38 |
| NC_000011.9:g.69464819C>T , CM000673.1:g.69464819C>T | GRCh37 |
| NC_000011.8:g.69174000C>T | NCBI36 |
| NG_007375.1:g.13947C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000227507.3:c.724-1067C>T MANE Select | ENSP00000227507.2:n.724-1067C>T | |
| ENST00000227507.2:c.724-1067C>T | ENSP00000227507.2:n.724-1067C>T | |
| ENST00000542367.1:n.187-1067C>T | ||
| NM_053056.2:c.724-1067C>T | NP_444284.1:n.724-1067C>T | |
| XM_006718653.2:c.748-1067C>T | XP_006718716.1:n.748-1067C>T | |
| NM_053056.3:c.724-1067C>T MANE Select | NP_444284.1:n.724-1067C>T |