Linked Data
dbSNP Id:
rs757895443
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.22114199G>C , CM000671.2:g.22114199G>C | GRCh38 |
| NC_000009.11:g.22114198G>C , CM000671.1:g.22114198G>C | GRCh37 |
| NC_000009.10:g.22104198G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_003529.3:n.2908+400G>C | ||
| NR_047532.1:n.1697+400G>C | ||
| NR_047534.1:n.961+400G>C | ||
| NR_047535.1:n.856+1804G>C | ||
| NR_047536.1:n.720+1804G>C | ||
| NR_047537.1:n.781-6001G>C | ||
| NR_047538.1:n.645-6001G>C | ||
| NR_047543.1:n.990+400G>C | ||
| NR_120536.1:n.645-6305G>C |