Linked Data
dbSNP Id:
rs1352341717
gnomAD v4:
11-1075535-T-C
MyVariant Identifiers:
chr11:g.1075535T>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.1075535T>C , CM000673.2:g.1075535T>C | GRCh38 |
| NC_000011.9:g.1075535T>C , CM000673.1:g.1075535T>C | GRCh37 |
| NC_000011.8:g.1065535T>C | NCBI36 |
| NG_051929.1:g.5661T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361558.7:n.104-116T>C | ||
| ENST00000675028.1:c.77-116T>C | ENSP00000502432.1:n.77-116T>C | |
| NM_002457.3:c.77-116T>C | NP_002448.3:n.77-116T>C | |
| NM_002457.4:c.77-116T>C | NP_002448.4:n.77-116T>C |