Linked Data
ClinVar Variation Id:
2746477
ClinVar RCV Id:
RCV003531105
dbSNP Id:
rs1221356278
gnomAD v2:
6-42937548-G-C
gnomAD v3:
6-42969810-G-C
gnomAD v4:
6-42969810-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.42969810G>C , CM000668.2:g.42969810G>C | GRCh38 |
| NC_000006.11:g.42937548G>C , CM000668.1:g.42937548G>C | GRCh37 |
| NC_000006.10:g.43045526G>C | NCBI36 |
| NG_008370.1:g.14434C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000304611.13:c.1234-9C>G MANE Select | ENSP00000303511.8:n.1234-9C>G | |
| ENST00000244546.4:c.1234-9C>G | ENSP00000244546.4:n.1234-9C>G | |
| ENST00000304611.12:c.1234-9C>G | ENSP00000303511.8:n.1234-9C>G | |
| NM_000287.3:c.1234-9C>G | NP_000278.3:n.1234-9C>G | |
| NM_001316313.1:c.970-9C>G | NP_001303242.1:n.970-9C>G | |
| NR_133009.1:n.1327-9C>G | ||
| XM_011514661.1:c.1150-9C>G | XP_011512963.1:n.1150-9C>G | |
| XR_926246.1:n.1327-9C>G | ||
| XM_011514661.2:c.1150-9C>G | XP_011512963.1:n.1150-9C>G | |
| XR_001743466.2:n.2308-9C>G | ||
| NM_000287.4:c.1234-9C>G MANE Select | NP_000278.3:n.1234-9C>G | |
| NM_001316313.2:c.970-9C>G | NP_001303242.1:n.970-9C>G | |
| NR_133009.2:n.1265-9C>G |